RU2013158080A - Пестицидные композиции и связанные с ними способы - Google Patents
Пестицидные композиции и связанные с ними способы Download PDFInfo
- Publication number
- RU2013158080A RU2013158080A RU2013158080/04A RU2013158080A RU2013158080A RU 2013158080 A RU2013158080 A RU 2013158080A RU 2013158080/04 A RU2013158080/04 A RU 2013158080/04A RU 2013158080 A RU2013158080 A RU 2013158080A RU 2013158080 A RU2013158080 A RU 2013158080A
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- Prior art keywords
- alkyl
- halogen
- alkoxy
- substituted
- methyl
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract 15
- 230000000361 pesticidal effect Effects 0.000 title 1
- 229910052736 halogen Inorganic materials 0.000 claims abstract 269
- 150000002367 halogens Chemical class 0.000 claims abstract 226
- 125000000217 alkyl group Chemical group 0.000 claims abstract 194
- 125000003545 alkoxy group Chemical group 0.000 claims abstract 183
- 125000001424 substituent group Chemical group 0.000 claims abstract 54
- 229910052801 chlorine Inorganic materials 0.000 claims abstract 53
- 229910052731 fluorine Inorganic materials 0.000 claims abstract 49
- 229910052794 bromium Inorganic materials 0.000 claims abstract 45
- 229910052740 iodine Inorganic materials 0.000 claims abstract 43
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 33
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims 149
- -1 (C = O) OH Chemical group 0.000 claims 73
- 125000000623 heterocyclic group Chemical group 0.000 claims 72
- 239000000460 chlorine Substances 0.000 claims 50
- 125000003107 substituted aryl group Chemical group 0.000 claims 49
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 36
- 125000002877 alkyl aryl group Chemical group 0.000 claims 32
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 25
- 239000011734 sodium Substances 0.000 claims 20
- 229910052708 sodium Inorganic materials 0.000 claims 20
- 239000011591 potassium Substances 0.000 claims 15
- 229910052700 potassium Inorganic materials 0.000 claims 15
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims 14
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 13
- 125000004969 haloethyl group Chemical group 0.000 claims 13
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 10
- 125000002053 thietanyl group Chemical group 0.000 claims 9
- 125000006529 (C3-C6) alkyl group Chemical group 0.000 claims 8
- 125000003342 alkenyl group Chemical group 0.000 claims 7
- 238000000034 method Methods 0.000 claims 7
- 125000004076 pyridyl group Chemical group 0.000 claims 7
- 125000003118 aryl group Chemical group 0.000 claims 6
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 5
- 229910052799 carbon Inorganic materials 0.000 claims 5
- 150000001875 compounds Chemical class 0.000 claims 5
- 125000005843 halogen group Chemical group 0.000 claims 5
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 5
- 125000003386 piperidinyl group Chemical group 0.000 claims 5
- 125000001376 1,2,4-triazolyl group Chemical group N1N=C(N=C1)* 0.000 claims 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 4
- 241000238631 Hexapoda Species 0.000 claims 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 4
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims 4
- 241000607479 Yersinia pestis Species 0.000 claims 4
- 229910052744 lithium Inorganic materials 0.000 claims 4
- 125000002757 morpholinyl group Chemical group 0.000 claims 4
- 229910052757 nitrogen Inorganic materials 0.000 claims 4
- 229910052760 oxygen Inorganic materials 0.000 claims 4
- 229910052717 sulfur Inorganic materials 0.000 claims 4
- TWFZGCMQGLPBSX-UHFFFAOYSA-N Carbendazim Natural products C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 claims 3
- 241000196324 Embryophyta Species 0.000 claims 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims 3
- 239000005562 Glyphosate Substances 0.000 claims 3
- 239000005574 MCPA Substances 0.000 claims 3
- 239000002253 acid Substances 0.000 claims 3
- JNPZQRQPIHJYNM-UHFFFAOYSA-N carbendazim Chemical compound C1=C[CH]C2=NC(NC(=O)OC)=NC2=C1 JNPZQRQPIHJYNM-UHFFFAOYSA-N 0.000 claims 3
- 239000006013 carbendazim Substances 0.000 claims 3
- 229940097068 glyphosate Drugs 0.000 claims 3
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims 3
- 150000007857 hydrazones Chemical class 0.000 claims 3
- JLIDBLDQVAYHNE-YKALOCIXSA-N (+)-Abscisic acid Chemical compound OC(=O)/C=C(/C)\C=C\[C@@]1(O)C(C)=CC(=O)CC1(C)C JLIDBLDQVAYHNE-YKALOCIXSA-N 0.000 claims 2
- XMGQYMWWDOXHJM-JTQLQIEISA-N (+)-α-limonene Chemical compound CC(=C)[C@@H]1CCC(C)=CC1 XMGQYMWWDOXHJM-JTQLQIEISA-N 0.000 claims 2
- SNICXCGAKADSCV-JTQLQIEISA-N (-)-Nicotine Chemical compound CN1CCC[C@H]1C1=CC=CN=C1 SNICXCGAKADSCV-JTQLQIEISA-N 0.000 claims 2
- KAATUXNTWXVJKI-NSHGMRRFSA-N (1R)-cis-(alphaS)-cypermethrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-NSHGMRRFSA-N 0.000 claims 2
- OTKXWJHPGBRXCR-UHFFFAOYSA-N (2-chloro-4-nitrophenoxy)-dimethoxy-sulfanylidene-$l^{5}-phosphane Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C=C1Cl OTKXWJHPGBRXCR-UHFFFAOYSA-N 0.000 claims 2
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 claims 2
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 claims 2
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 claims 2
- WURBVZBTWMNKQT-UHFFFAOYSA-N 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C1=NC=NN1C(C(=O)C(C)(C)C)OC1=CC=C(Cl)C=C1 WURBVZBTWMNKQT-UHFFFAOYSA-N 0.000 claims 2
- HZTCLDNADGMACV-UHFFFAOYSA-N 1-(8-hydroxyquinolin-5-yl)ethanone Chemical compound C1=CC=C2C(C(=O)C)=CC=C(O)C2=N1 HZTCLDNADGMACV-UHFFFAOYSA-N 0.000 claims 2
- PZBPKYOVPCNPJY-UHFFFAOYSA-N 1-[2-(allyloxy)-2-(2,4-dichlorophenyl)ethyl]imidazole Chemical compound ClC1=CC(Cl)=CC=C1C(OCC=C)CN1C=NC=C1 PZBPKYOVPCNPJY-UHFFFAOYSA-N 0.000 claims 2
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 claims 2
- FMTFEIJHMMQUJI-NJAFHUGGSA-N 102130-98-3 Natural products CC=CCC1=C(C)[C@H](CC1=O)OC(=O)[C@@H]1[C@@H](C=C(C)C)C1(C)C FMTFEIJHMMQUJI-NJAFHUGGSA-N 0.000 claims 2
- WNTGYJSOUMFZEP-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-UHFFFAOYSA-N 0.000 claims 2
- YCCILVSKPBXVIP-UHFFFAOYSA-N 2-(4-hydroxyphenyl)ethanol Chemical compound OCCC1=CC=C(O)C=C1 YCCILVSKPBXVIP-UHFFFAOYSA-N 0.000 claims 2
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 claims 2
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims 2
- RQRMKMRFKZIYOG-UHFFFAOYSA-N 3-[(6-chloropyridin-3-yl)methyl-methylamino]-2h-furan-5-one Chemical compound C=1C(=O)OCC=1N(C)CC1=CC=C(Cl)N=C1 RQRMKMRFKZIYOG-UHFFFAOYSA-N 0.000 claims 2
- ZXVONLUNISGICL-UHFFFAOYSA-N 4,6-dinitro-o-cresol Chemical compound CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O ZXVONLUNISGICL-UHFFFAOYSA-N 0.000 claims 2
- 241001124076 Aphididae Species 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- 241001674044 Blattodea Species 0.000 claims 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims 2
- 101150065749 Churc1 gene Proteins 0.000 claims 2
- FMTFEIJHMMQUJI-UHFFFAOYSA-N Cinerin I Natural products C1C(=O)C(CC=CC)=C(C)C1OC(=O)C1C(C)(C)C1C=C(C)C FMTFEIJHMMQUJI-UHFFFAOYSA-N 0.000 claims 2
- 241000723346 Cinnamomum camphora Species 0.000 claims 2
- 229920000742 Cotton Polymers 0.000 claims 2
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 claims 2
- 241000255925 Diptera Species 0.000 claims 2
- 239000005630 Diquat Substances 0.000 claims 2
- 239000005558 Fluroxypyr Substances 0.000 claims 2
- 241000258937 Hemiptera Species 0.000 claims 2
- RWNKSTSCBHKHTB-UHFFFAOYSA-N Hexachloro-1,3-butadiene Chemical compound ClC(Cl)=C(Cl)C(Cl)=C(Cl)Cl RWNKSTSCBHKHTB-UHFFFAOYSA-N 0.000 claims 2
- 241000257303 Hymenoptera Species 0.000 claims 2
- 241000256602 Isoptera Species 0.000 claims 2
- QVJMXSGZTCGLHZ-VWADHSNXSA-N Juvenile hormone III Natural products O=C(OC)/C=C(\CC/C=C(\CC[C@H]1C(C)(C)O1)/C)/C QVJMXSGZTCGLHZ-VWADHSNXSA-N 0.000 claims 2
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 claims 2
- 241000255777 Lepidoptera Species 0.000 claims 2
- 239000005575 MCPB Substances 0.000 claims 2
- 101150039283 MCPB gene Proteins 0.000 claims 2
- 239000002169 Metam Substances 0.000 claims 2
- LVPGGWVHPIAEMC-UHFFFAOYSA-L Morfamquat Chemical compound [Cl-].[Cl-].CC1COCC(C)N1C(=O)C[N+]1=CC=C(C=2C=C[N+](CC(=O)N3C(COCC3C)C)=CC=2)C=C1 LVPGGWVHPIAEMC-UHFFFAOYSA-L 0.000 claims 2
- KJHOZAZQWVKILO-UHFFFAOYSA-N N-(diaminomethylidene)-4-morpholinecarboximidamide Chemical compound NC(N)=NC(=N)N1CCOCC1 KJHOZAZQWVKILO-UHFFFAOYSA-N 0.000 claims 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims 2
- 241000244206 Nematoda Species 0.000 claims 2
- CVRALZAYCYJELZ-UHFFFAOYSA-N O-(4-bromo-2,5-dichlorophenyl) O-methyl phenylphosphonothioate Chemical compound C=1C=CC=CC=1P(=S)(OC)OC1=CC(Cl)=C(Br)C=C1Cl CVRALZAYCYJELZ-UHFFFAOYSA-N 0.000 claims 2
- 241000238814 Orthoptera Species 0.000 claims 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims 2
- 241001674048 Phthiraptera Species 0.000 claims 2
- 102100038239 Protein Churchill Human genes 0.000 claims 2
- INVGWHRKADIJHF-UHFFFAOYSA-N Sanguinarin Chemical compound C1=C2OCOC2=CC2=C3[N+](C)=CC4=C(OCO5)C5=CC=C4C3=CC=C21 INVGWHRKADIJHF-UHFFFAOYSA-N 0.000 claims 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims 2
- 241000258242 Siphonaptera Species 0.000 claims 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 claims 2
- KWAIHLIXESXTJL-UHFFFAOYSA-N aminocyclopyrachlor Chemical compound OC(=O)C1=C(Cl)C(N)=NC(C2CC2)=N1 KWAIHLIXESXTJL-UHFFFAOYSA-N 0.000 claims 2
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- OTSAMNSACVKIOJ-UHFFFAOYSA-N azane;carbamoyl(ethoxy)phosphinic acid Chemical compound [NH4+].CCOP([O-])(=O)C(N)=O OTSAMNSACVKIOJ-UHFFFAOYSA-N 0.000 claims 2
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 claims 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 claims 2
- 239000011575 calcium Substances 0.000 claims 2
- 229910052791 calcium Inorganic materials 0.000 claims 2
- 229960000846 camphor Drugs 0.000 claims 2
- 229930008380 camphor Natural products 0.000 claims 2
- 239000002775 capsule Substances 0.000 claims 2
- ULDHMXUKGWMISQ-UHFFFAOYSA-N carvone Chemical compound CC(=C)C1CC=C(C)C(=O)C1 ULDHMXUKGWMISQ-UHFFFAOYSA-N 0.000 claims 2
- PNCNFDRSHBFIDM-WOJGMQOQSA-N chembl111617 Chemical compound C=CCO\N=C(/CCC)C1=C(O)C(C(=O)OC)C(C)(C)CC1=O PNCNFDRSHBFIDM-WOJGMQOQSA-N 0.000 claims 2
- 125000006378 chloropyridyl group Chemical group 0.000 claims 2
- FMTFEIJHMMQUJI-DFKXKMKHSA-N cinerin I Chemical compound C1C(=O)C(C\C=C/C)=C(C)[C@H]1OC(=O)[C@H]1C(C)(C)[C@@H]1C=C(C)C FMTFEIJHMMQUJI-DFKXKMKHSA-N 0.000 claims 2
- 239000010949 copper Substances 0.000 claims 2
- 229910052802 copper Inorganic materials 0.000 claims 2
- MZZBPDKVEFVLFF-UHFFFAOYSA-N cyanazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C#N)=N1 MZZBPDKVEFVLFF-UHFFFAOYSA-N 0.000 claims 2
- YPHMISFOHDHNIV-FSZOTQKASA-N cycloheximide Chemical compound C1[C@@H](C)C[C@H](C)C(=O)[C@@H]1[C@H](O)CC1CC(=O)NC(=O)C1 YPHMISFOHDHNIV-FSZOTQKASA-N 0.000 claims 2
- 230000001419 dependent effect Effects 0.000 claims 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 claims 2
- DFBKLUNHFCTMDC-PICURKEMSA-N dieldrin Chemical compound C([C@H]1[C@H]2[C@@]3(Cl)C(Cl)=C([C@]([C@H]22)(Cl)C3(Cl)Cl)Cl)[C@H]2[C@@H]2[C@H]1O2 DFBKLUNHFCTMDC-PICURKEMSA-N 0.000 claims 2
- WGWJBWHBOKETRC-UHFFFAOYSA-N diethoxy-(3-methyl-4-methylsulfanylphenoxy)-sulfanylidene-$l^{5}-phosphane Chemical compound CCOP(=S)(OCC)OC1=CC=C(SC)C(C)=C1 WGWJBWHBOKETRC-UHFFFAOYSA-N 0.000 claims 2
- FBOUIAKEJMZPQG-BLXFFLACSA-N diniconazole-M Chemical compound C1=NC=NN1/C([C@H](O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1Cl FBOUIAKEJMZPQG-BLXFFLACSA-N 0.000 claims 2
- 229950010286 diolamine Drugs 0.000 claims 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims 2
- KZTYYGOKRVBIMI-UHFFFAOYSA-N diphenyl sulfone Chemical compound C=1C=CC=CC=1S(=O)(=O)C1=CC=CC=C1 KZTYYGOKRVBIMI-UHFFFAOYSA-N 0.000 claims 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 claims 2
- AUZONCFQVSMFAP-UHFFFAOYSA-N disulfiram Chemical compound CCN(CC)C(=S)SSC(=S)N(CC)CC AUZONCFQVSMFAP-UHFFFAOYSA-N 0.000 claims 2
- GCKZANITAMOIAR-XWVCPFKXSA-N dsstox_cid_14566 Chemical compound [O-]C(=O)C1=CC=CC=C1.C1=C[C@H](C)[C@@H]([C@@H](C)CC)O[C@]11O[C@H](C\C=C(C)\[C@@H](O[C@@H]2O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H]([NH2+]C)[C@@H](OC)C3)[C@@H](OC)C2)[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 GCKZANITAMOIAR-XWVCPFKXSA-N 0.000 claims 2
- 229960002125 enilconazole Drugs 0.000 claims 2
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- 125000001207 fluorophenyl group Chemical group 0.000 claims 2
- MEFQWPUMEMWTJP-UHFFFAOYSA-N fluroxypyr Chemical compound NC1=C(Cl)C(F)=NC(OCC(O)=O)=C1Cl MEFQWPUMEMWTJP-UHFFFAOYSA-N 0.000 claims 2
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 claims 2
- 229960003692 gamma aminobutyric acid Drugs 0.000 claims 2
- BTCSSZJGUNDROE-UHFFFAOYSA-N gamma-aminobutyric acid Chemical compound NCCCC(O)=O BTCSSZJGUNDROE-UHFFFAOYSA-N 0.000 claims 2
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- RONFGUROBZGJKP-UHFFFAOYSA-N iminoctadine Chemical compound NC(N)=NCCCCCCCCNCCCCCCCCN=C(N)N RONFGUROBZGJKP-UHFFFAOYSA-N 0.000 claims 2
- 239000003112 inhibitor Substances 0.000 claims 2
- ZNJFBWYDHIGLCU-HWKXXFMVSA-N jasmonic acid Chemical compound CC\C=C/C[C@@H]1[C@@H](CC(O)=O)CCC1=O ZNJFBWYDHIGLCU-HWKXXFMVSA-N 0.000 claims 2
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- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Natural products CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 claims 2
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 claims 2
- FIKAKWIAUPDISJ-UHFFFAOYSA-L paraquat dichloride Chemical compound [Cl-].[Cl-].C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 FIKAKWIAUPDISJ-UHFFFAOYSA-L 0.000 claims 2
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 claims 2
- JPFWJDMDPLEUBD-ITJAGOAWSA-N polyoxorim Polymers O[C@@H]1[C@H](O)[C@@H]([C@H](NC(=O)[C@H]([C@H](O)[C@@H](O)COC(N)=O)N)C(O)=O)O[C@H]1N1C(=O)NC(=O)C(C(O)=O)=C1 JPFWJDMDPLEUBD-ITJAGOAWSA-N 0.000 claims 2
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- 150000008117 polysulfides Polymers 0.000 claims 2
- CPTJXGLQLVPIGP-UHFFFAOYSA-N precocene I Chemical compound C1=CC(C)(C)OC2=CC(OC)=CC=C21 CPTJXGLQLVPIGP-UHFFFAOYSA-N 0.000 claims 2
- WTFXJFJYEJZMFO-UHFFFAOYSA-N propamidine Chemical compound C1=CC(C(=N)N)=CC=C1OCCCOC1=CC=C(C(N)=N)C=C1 WTFXJFJYEJZMFO-UHFFFAOYSA-N 0.000 claims 2
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- MDXGYOOITGBCBW-UHFFFAOYSA-N methyl 2-[4-[4-(trifluoromethyl)phenoxy]phenoxy]propanoate Chemical group C1=CC(OC(C)C(=O)OC)=CC=C1OC1=CC=C(C(F)(F)F)C=C1 MDXGYOOITGBCBW-UHFFFAOYSA-N 0.000 claims 1
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- RTWIRLHWLMNVCC-WQYNNSOESA-M sodium (2S)-2-[[(2S)-2-[[(2S)-2-amino-4-[hydroxy(methyl)phosphoryl]butanoyl]amino]propanoyl]amino]propanoate Chemical compound [Na+].[O-]C(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@@H](N)CCP(C)(O)=O RTWIRLHWLMNVCC-WQYNNSOESA-M 0.000 claims 1
- PTLRDCMBXHILCL-UHFFFAOYSA-M sodium arsenite Chemical compound [Na+].[O-][As]=O PTLRDCMBXHILCL-UHFFFAOYSA-M 0.000 claims 1
- HYHCSLBZRBJJCH-UHFFFAOYSA-N sodium polysulfide Chemical compound [Na+].S HYHCSLBZRBJJCH-UHFFFAOYSA-N 0.000 claims 1
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- SGUSXTMVKMPQKI-UHFFFAOYSA-M sodium;2,2,3,3-tetrafluoropropanoate Chemical compound [Na+].[O-]C(=O)C(F)(F)C(F)F SGUSXTMVKMPQKI-UHFFFAOYSA-M 0.000 claims 1
- HCJLVWUMMKIQIM-UHFFFAOYSA-M sodium;2,3,4,5,6-pentachlorophenolate Chemical compound [Na+].[O-]C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl HCJLVWUMMKIQIM-UHFFFAOYSA-M 0.000 claims 1
- PPRNMFDWJLACKG-UHFFFAOYSA-N sodium;2-(2,2-dimethylpropanoyl)inden-2-ide-1,3-dione Chemical compound [Na+].C1=CC=C2C(=O)[C-](C(=O)C(C)(C)C)C(=O)C2=C1 PPRNMFDWJLACKG-UHFFFAOYSA-N 0.000 claims 1
- KISFEBPWFCGRGN-UHFFFAOYSA-M sodium;2-(2,4-dichlorophenoxy)ethyl sulfate Chemical compound [Na+].[O-]S(=O)(=O)OCCOC1=CC=C(Cl)C=C1Cl KISFEBPWFCGRGN-UHFFFAOYSA-M 0.000 claims 1
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- JUNDBKFAZXZKRA-MAFYXNADSA-M sodium;2-[(e)-n-[(3,5-difluorophenyl)carbamoylamino]-c-methylcarbonimidoyl]pyridine-3-carboxylate Chemical compound [Na+].N=1C=CC=C(C([O-])=O)C=1C(/C)=N/NC(=O)NC1=CC(F)=CC(F)=C1 JUNDBKFAZXZKRA-MAFYXNADSA-M 0.000 claims 1
- XKKTVIWAHIWFAN-UHFFFAOYSA-M sodium;2-[2-[2-(dodecylamino)ethylamino]ethylamino]acetate Chemical compound [Na+].CCCCCCCCCCCCNCCNCCNCC([O-])=O XKKTVIWAHIWFAN-UHFFFAOYSA-M 0.000 claims 1
- LRWSMDCIWRLZIX-UHFFFAOYSA-M sodium;2-butan-2-yl-4,6-dinitrophenolate Chemical compound [Na+].CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1[O-] LRWSMDCIWRLZIX-UHFFFAOYSA-M 0.000 claims 1
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- JQYJSVBNPUHHKB-UHFFFAOYSA-M sodium;2-methyl-4,6-dinitrophenolate Chemical compound [Na+].CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1[O-] JQYJSVBNPUHHKB-UHFFFAOYSA-M 0.000 claims 1
- KYITYFHKDODNCQ-UHFFFAOYSA-M sodium;2-oxo-3-(3-oxo-1-phenylbutyl)chromen-4-olate Chemical compound [Na+].[O-]C=1C2=CC=CC=C2OC(=O)C=1C(CC(=O)C)C1=CC=CC=C1 KYITYFHKDODNCQ-UHFFFAOYSA-M 0.000 claims 1
- KQSJSRIUULBTSE-UHFFFAOYSA-M sodium;3-(3-ethylcyclopentyl)propanoate Chemical compound [Na+].CCC1CCC(CCC([O-])=O)C1 KQSJSRIUULBTSE-UHFFFAOYSA-M 0.000 claims 1
- GABUSZPTCJGKGB-UHFFFAOYSA-M sodium;4-(4-chloro-2-methylphenoxy)butanoate Chemical compound [Na+].CC1=CC(Cl)=CC=C1OCCCC([O-])=O GABUSZPTCJGKGB-UHFFFAOYSA-M 0.000 claims 1
- QGKPUZOFTJQTHL-UHFFFAOYSA-M sodium;4-cyano-2,6-diiodophenolate Chemical compound [Na+].[O-]C1=C(I)C=C(C#N)C=C1I QGKPUZOFTJQTHL-UHFFFAOYSA-M 0.000 claims 1
- 229940014213 spinosad Drugs 0.000 claims 1
- DTDSAWVUFPGDMX-UHFFFAOYSA-N spirodiclofen Chemical compound CCC(C)(C)C(=O)OC1=C(C=2C(=CC(Cl)=CC=2)Cl)C(=O)OC11CCCCC1 DTDSAWVUFPGDMX-UHFFFAOYSA-N 0.000 claims 1
- PUYXTUJWRLOUCW-UHFFFAOYSA-N spiroxamine Chemical compound O1C(CN(CC)CCC)COC11CCC(C(C)(C)C)CC1 PUYXTUJWRLOUCW-UHFFFAOYSA-N 0.000 claims 1
- 235000021012 strawberries Nutrition 0.000 claims 1
- 229960005322 streptomycin Drugs 0.000 claims 1
- QTENRWWVYAAPBI-YCRXJPFRSA-N streptomycin sulfate Chemical compound OS(O)(=O)=O.OS(O)(=O)=O.OS(O)(=O)=O.CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](N=C(N)N)[C@H](O)[C@@H](N=C(N)N)[C@H](O)[C@H]1O.CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](N=C(N)N)[C@H](O)[C@@H](N=C(N)N)[C@H](O)[C@H]1O QTENRWWVYAAPBI-YCRXJPFRSA-N 0.000 claims 1
- 229960005453 strychnine Drugs 0.000 claims 1
- PQTBTIFWAXVEPB-UHFFFAOYSA-N sulcotrione Chemical compound ClC1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O PQTBTIFWAXVEPB-UHFFFAOYSA-N 0.000 claims 1
- OORLZFUTLGXMEF-UHFFFAOYSA-N sulfentrazone Chemical compound O=C1N(C(F)F)C(C)=NN1C1=CC(NS(C)(=O)=O)=C(Cl)C=C1Cl OORLZFUTLGXMEF-UHFFFAOYSA-N 0.000 claims 1
- CTPKSRZFJSJGML-UHFFFAOYSA-N sulfiram Chemical compound CCN(CC)C(=S)SC(=S)N(CC)CC CTPKSRZFJSJGML-UHFFFAOYSA-N 0.000 claims 1
- 229950008316 sulfiram Drugs 0.000 claims 1
- FZMKKCQHDROFNI-UHFFFAOYSA-N sulfometuron Chemical compound CC1=CC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 FZMKKCQHDROFNI-UHFFFAOYSA-N 0.000 claims 1
- 150000003462 sulfoxides Chemical class 0.000 claims 1
- 239000005936 tau-Fluvalinate Substances 0.000 claims 1
- INISTDXBRIBGOC-XMMISQBUSA-N tau-fluvalinate Chemical compound N([C@H](C(C)C)C(=O)OC(C#N)C=1C=C(OC=2C=CC=CC=2)C=CC=1)C1=CC=C(C(F)(F)F)C=C1Cl INISTDXBRIBGOC-XMMISQBUSA-N 0.000 claims 1
- LWLJEQHTPVPKSJ-UHFFFAOYSA-N tebufloquin Chemical compound C1=C(C(C)(C)C)C=C2C(OC(=O)C)=C(C)C(C)=NC2=C1F LWLJEQHTPVPKSJ-UHFFFAOYSA-N 0.000 claims 1
- XQTLDIFVVHJORV-UHFFFAOYSA-N tecnazene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl XQTLDIFVVHJORV-UHFFFAOYSA-N 0.000 claims 1
- CJDWRQLODFKPEL-UHFFFAOYSA-N teflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC(Cl)=C(F)C(Cl)=C1F CJDWRQLODFKPEL-UHFFFAOYSA-N 0.000 claims 1
- IUQAXCIUEPFPSF-UHFFFAOYSA-N tembotrione Chemical compound ClC1=C(COCC(F)(F)F)C(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O IUQAXCIUEPFPSF-UHFFFAOYSA-N 0.000 claims 1
- BCQMBFHBDZVHKU-UHFFFAOYSA-N terbumeton Chemical compound CCNC1=NC(NC(C)(C)C)=NC(OC)=N1 BCQMBFHBDZVHKU-UHFFFAOYSA-N 0.000 claims 1
- FZXISNSWEXTPMF-UHFFFAOYSA-N terbutylazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C)=N1 FZXISNSWEXTPMF-UHFFFAOYSA-N 0.000 claims 1
- IWVCMVBTMGNXQD-UHFFFAOYSA-N terramycin dehydrate Natural products C1=CC=C2C(O)(C)C3C(O)C4C(N(C)C)C(O)=C(C(N)=O)C(=O)C4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-UHFFFAOYSA-N 0.000 claims 1
- DPOWHSMECVNHAT-YERPJTIDSA-N tetcyclacis Chemical compound C1=CC(Cl)=CC=C1N1[C@H]2[C@H]([C@@H]3[C@H]4N=N3)C[C@H]4[C@H]2N=N1 DPOWHSMECVNHAT-YERPJTIDSA-N 0.000 claims 1
- UGNWTBMOAKPKBL-UHFFFAOYSA-N tetrachloro-1,4-benzoquinone Chemical compound ClC1=C(Cl)C(=O)C(Cl)=C(Cl)C1=O UGNWTBMOAKPKBL-UHFFFAOYSA-N 0.000 claims 1
- UBCKGWBNUIFUST-YHYXMXQVSA-N tetrachlorvinphos Chemical compound COP(=O)(OC)O\C(=C/Cl)C1=CC(Cl)=C(Cl)C=C1Cl UBCKGWBNUIFUST-YHYXMXQVSA-N 0.000 claims 1
- 229960005199 tetramethrin Drugs 0.000 claims 1
- AGGKEGLBGGJEBZ-UHFFFAOYSA-N tetramethylenedisulfotetramine Chemical compound C1N(S2(=O)=O)CN3S(=O)(=O)N1CN2C3 AGGKEGLBGGJEBZ-UHFFFAOYSA-N 0.000 claims 1
- YTQVHRVITVLIRD-UHFFFAOYSA-L thallium sulfate Chemical compound [Tl+].[Tl+].[O-]S([O-])(=O)=O YTQVHRVITVLIRD-UHFFFAOYSA-L 0.000 claims 1
- 229940119523 thallium sulfate Drugs 0.000 claims 1
- 229910000374 thallium(I) sulfate Inorganic materials 0.000 claims 1
- 239000004308 thiabendazole Substances 0.000 claims 1
- 229960004546 thiabendazole Drugs 0.000 claims 1
- 235000010296 thiabendazole Nutrition 0.000 claims 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 claims 1
- NWWZPOKUUAIXIW-FLIBITNWSA-N thiamethoxam Chemical compound [O-][N+](=O)\N=C/1N(C)COCN\1CC1=CN=C(Cl)S1 NWWZPOKUUAIXIW-FLIBITNWSA-N 0.000 claims 1
- GLDAZAQRGCSFNP-UHFFFAOYSA-N thiencarbazone Chemical compound O=C1N(C)C(OC)=NN1C(=O)NS(=O)(=O)C1=C(C)SC=C1C(O)=O GLDAZAQRGCSFNP-UHFFFAOYSA-N 0.000 claims 1
- XSKZXGDFSCCXQX-UHFFFAOYSA-N thiencarbazone-methyl Chemical group COC(=O)C1=CSC(C)=C1S(=O)(=O)NC(=O)N1C(=O)N(C)C(OC)=N1 XSKZXGDFSCCXQX-UHFFFAOYSA-N 0.000 claims 1
- RTKIYNMVFMVABJ-UHFFFAOYSA-L thimerosal Chemical compound [Na+].CC[Hg]SC1=CC=CC=C1C([O-])=O RTKIYNMVFMVABJ-UHFFFAOYSA-L 0.000 claims 1
- SRVJKTDHMYAMHA-WUXMJOGZSA-N thioacetazone Chemical group CC(=O)NC1=CC=C(\C=N\NC(N)=S)C=C1 SRVJKTDHMYAMHA-WUXMJOGZSA-N 0.000 claims 1
- 229960003231 thioacetazone Drugs 0.000 claims 1
- DNVLJEWNNDHELH-UHFFFAOYSA-N thiocyclam Chemical compound CN(C)C1CSSSC1 DNVLJEWNNDHELH-UHFFFAOYSA-N 0.000 claims 1
- DYLDNPYVDMQCFR-UHFFFAOYSA-N thiocyclam hydrochloride Chemical compound Cl.CN(C)C1CSSSC1 DYLDNPYVDMQCFR-UHFFFAOYSA-N 0.000 claims 1
- ICTQUFQQEYSGGJ-UHFFFAOYSA-N thiocyclam oxalate Chemical compound OC(=O)C(O)=O.CN(C)C1CSSSC1 ICTQUFQQEYSGGJ-UHFFFAOYSA-N 0.000 claims 1
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- HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-N 0.000 claims 1
- 230000000699 topical effect Effects 0.000 claims 1
- IYMLUHWAJFXAQP-UHFFFAOYSA-N topramezone Chemical compound CC1=C(C(=O)C2=C(N(C)N=C2)O)C=CC(S(C)(=O)=O)=C1C1=NOCC1 IYMLUHWAJFXAQP-UHFFFAOYSA-N 0.000 claims 1
- UZKQTCBAMSWPJD-UQCOIBPSSA-N trans-Zeatin Natural products OCC(/C)=C\CNC1=NC=NC2=C1N=CN2 UZKQTCBAMSWPJD-UQCOIBPSSA-N 0.000 claims 1
- UZKQTCBAMSWPJD-FARCUNLSSA-N trans-zeatin Chemical compound OCC(/C)=C/CNC1=NC=NC2=C1N=CN2 UZKQTCBAMSWPJD-FARCUNLSSA-N 0.000 claims 1
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- 229950001353 tretamine Drugs 0.000 claims 1
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 claims 1
- NKNFWVNSBIXGLL-UHFFFAOYSA-N triazamate Chemical compound CCOC(=O)CSC1=NC(C(C)(C)C)=NN1C(=O)N(C)C NKNFWVNSBIXGLL-UHFFFAOYSA-N 0.000 claims 1
- AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 claims 1
- IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 claims 1
- BQZXUHDXIARLEO-UHFFFAOYSA-N tribenuron Chemical compound COC1=NC(C)=NC(N(C)C(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 BQZXUHDXIARLEO-UHFFFAOYSA-N 0.000 claims 1
- YMXOXAPKZDWXLY-QWRGUYRKSA-N tribenuron methyl Chemical group COC(=O)[C@H]1CCCC[C@@H]1S(=O)(=O)NC(=O)N(C)C1=NC(C)=NC(OC)=N1 YMXOXAPKZDWXLY-QWRGUYRKSA-N 0.000 claims 1
- WCLDITPGPXSPGV-UHFFFAOYSA-N tricamba Chemical compound COC1=C(Cl)C=C(Cl)C(Cl)=C1C(O)=O WCLDITPGPXSPGV-UHFFFAOYSA-N 0.000 claims 1
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 claims 1
- NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 claims 1
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 claims 1
- ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-N 0.000 claims 1
- XAIPTRIXGHTTNT-UHFFFAOYSA-N triflumuron Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)NC(=O)C1=CC=CC=C1Cl XAIPTRIXGHTTNT-UHFFFAOYSA-N 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- MWKJTNBSKNUMFN-UHFFFAOYSA-N trifluoromethyltrimethylsilane Chemical compound C[Si](C)(C)C(F)(F)F MWKJTNBSKNUMFN-UHFFFAOYSA-N 0.000 claims 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 claims 1
- AKTQJCBOGPBERP-UHFFFAOYSA-N triflusulfuron Chemical compound FC(F)(F)COC1=NC(N(C)C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2C)C(O)=O)=N1 AKTQJCBOGPBERP-UHFFFAOYSA-N 0.000 claims 1
- IMEVJVISCHQJRM-UHFFFAOYSA-N triflusulfuron-methyl Chemical group COC(=O)C1=CC=CC(C)=C1S(=O)(=O)NC(=O)NC1=NC(OCC(F)(F)F)=NC(N(C)C)=N1 IMEVJVISCHQJRM-UHFFFAOYSA-N 0.000 claims 1
- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 claims 1
- RVKCCVTVZORVGD-UHFFFAOYSA-N trinexapac-ethyl Chemical group O=C1CC(C(=O)OCC)CC(=O)C1=C(O)C1CC1 RVKCCVTVZORVGD-UHFFFAOYSA-N 0.000 claims 1
- YKUJZZHGTWVWHA-UHFFFAOYSA-N triptolide Natural products COC12CC3OC3(C(C)C)C(O)C14OC4CC5C6=C(CCC25C)C(=O)OC6 YKUJZZHGTWVWHA-UHFFFAOYSA-N 0.000 claims 1
- KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 claims 1
- 235000013976 turmeric Nutrition 0.000 claims 1
- YNWVFADWVLCOPU-MAUPQMMJSA-N uniconazole P Chemical compound C1=NC=NN1/C([C@@H](O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1 YNWVFADWVLCOPU-MAUPQMMJSA-N 0.000 claims 1
- 229940070710 valerate Drugs 0.000 claims 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 claims 1
- JARYYMUOCXVXNK-IMTORBKUSA-N validamycin Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-IMTORBKUSA-N 0.000 claims 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 1
- 229920002554 vinyl polymer Polymers 0.000 claims 1
- 230000003253 viricidal effect Effects 0.000 claims 1
- MECHNRXZTMCUDQ-RKHKHRCZSA-N vitamin D2 Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)/C=C/[C@H](C)C(C)C)=C\C=C1\C[C@@H](O)CCC1=C MECHNRXZTMCUDQ-RKHKHRCZSA-N 0.000 claims 1
- 235000001892 vitamin D2 Nutrition 0.000 claims 1
- 239000011653 vitamin D2 Substances 0.000 claims 1
- 229960005080 warfarin Drugs 0.000 claims 1
- PJVWKTKQMONHTI-UHFFFAOYSA-N warfarin Chemical compound OC=1C2=CC=CC=C2OC(=O)C=1C(CC(=O)C)C1=CC=CC=C1 PJVWKTKQMONHTI-UHFFFAOYSA-N 0.000 claims 1
- 229960000883 warfarin potassium Drugs 0.000 claims 1
- 229960002647 warfarin sodium Drugs 0.000 claims 1
- 150000003739 xylenols Chemical class 0.000 claims 1
- 229940023877 zeatin Drugs 0.000 claims 1
- 239000005943 zeta-Cypermethrin Substances 0.000 claims 1
- 229940048462 zinc phosphide Drugs 0.000 claims 1
- FJBGIXKIXPUXBY-UHFFFAOYSA-N {2-[3-(4-chlorophenyl)propyl]-2,4,4-trimethyl-1,3-oxazolidin-3-yl}(imidazol-1-yl)methanone Chemical compound C1=CN=CN1C(=O)N1C(C)(C)COC1(C)CCCC1=CC=C(Cl)C=C1 FJBGIXKIXPUXBY-UHFFFAOYSA-N 0.000 claims 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/02—Amines; Quaternary ammonium compounds
- A01N33/04—Nitrogen directly attached to aliphatic or cycloaliphatic carbon atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds containing nitrogen-to-oxygen bonds
- A01N33/24—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds containing nitrogen-to-oxygen bonds only one oxygen atom attached to the nitrogen atom
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- A01N35/06—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical containing keto or thioketo groups as part of a ring, e.g. cyclohexanone, quinone; Derivatives thereof, e.g. ketals
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- A01N35/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical at least one of the bonds to hetero atoms is to nitrogen
- A01N35/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical at least one of the bonds to hetero atoms is to nitrogen containing a carbon-to-nitrogen double bond
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/10—Aromatic or araliphatic carboxylic acids, or thio analogues thereof; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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Abstract
1. Композиция, содержащая молекулу формулы один:где:(a) R1 выбран из(1) H, F, Cl, Br, I, CN, NO, (C-C)алкила, галоген(C-C)алкила, (C-C)алкокси, галоген(C-C)алкокси, S(C-C)алкила, S(галоген(C-C)алкил), S(O)(C-C)алкила, S(O)(галоген(C-C)алкил), S(O)(C-C)алкила, S(O)(галоген(C-C)алкил), N(R14)(R15),(2) замещенного (C-C)алкила, где указанный замещенный (C-C)алкил содержит один или несколько заместителей, выбранных из CN и NO,(3) замещенного галоген(C-C)алкила, где указанный замещенный галоген(C-C)алкил содержит один или несколько заместителей, выбранных из CN и NO,(4) замещенного (C-C)алкокси, где указанный замещенный (C-C)алкокси содержит один или несколько заместителей, выбранных из CN и NO, и(5) замещенного галоген(C-C)алкокси, где указанный замещенный галоген(C-C)алкокси содержит один или несколько заместителей, выбранных из CN и NO;(b) R2 выбран из(1) H, F, Cl, Br, I, CN, NO, (C-C)алкила, галоген(C-C)алкила, (C-C)алкокси, галоген(C-C)алкокси, S(C-C)алкила, S(галоген(C-C)алкил), S(O)(C-C)алкила, S(O)(галоген(C-C)алкил), S(O)(C-C)алкила, S(O)(галоген(C-C)алкил), N(R14)(R15),(2) замещенного (C-C)алкила, где указанный замещенный (C-C)алкил содержит один или несколько заместителей, выбранных из CN и NO,(3) замещенного галоген(C-C)алкила, где указанный замещенный галоген(C-C)алкил содержит один или несколько заместителей, выбранных из CN и NO,(4) замещенного (C-C)алкокси, где указанный замещенный (C-C)алкокси содержит один или несколько заместителей, выбранных из CN и NO, и(5) замещенного галоген(C-C)алкокси, где указанный замещенный галоген(C-C)алкокси содержит один или несколько заместителей, выбранных из CN и NO;(c) R3 выбран из(1) H, F, Cl, Br, I, CN, NO, (C-C)алкила, галоген(C-C)алкила, (C-C)алкокси, галоген(C-C)алкокси, S(C-C)алкила, S(галоген(C-C)алкил), S(O)(C-C)алкила, S(O)(галоген(C-C)алкил), S(O)(C-C)алкила, S(O)(гал�
Claims (15)
1. Композиция, содержащая молекулу формулы один:
где:
(a) R1 выбран из
(1) H, F, Cl, Br, I, CN, NO2, (C1-C8)алкила, галоген(C1-C8)алкила, (C1-C8)алкокси, галоген(C1-C8)алкокси, S(C1-C8)алкила, S(галоген(C1-C8)алкил), S(O)(C1-C8)алкила, S(O)(галоген(C1-C8)алкил), S(O)2(C1-C8)алкила, S(O)2(галоген(C1-C8)алкил), N(R14)(R15),
(2) замещенного (C1-C8)алкила, где указанный замещенный (C1-C8)алкил содержит один или несколько заместителей, выбранных из CN и NO2,
(3) замещенного галоген(C1-C8)алкила, где указанный замещенный галоген(C1-C8)алкил содержит один или несколько заместителей, выбранных из CN и NO2,
(4) замещенного (C1-C8)алкокси, где указанный замещенный (C1-C8)алкокси содержит один или несколько заместителей, выбранных из CN и NO2, и
(5) замещенного галоген(C1-C8)алкокси, где указанный замещенный галоген(C1-C8)алкокси содержит один или несколько заместителей, выбранных из CN и NO2;
(b) R2 выбран из
(1) H, F, Cl, Br, I, CN, NO2, (C1-C8)алкила, галоген(C1-C8)алкила, (C1-C8)алкокси, галоген(C1-C8)алкокси, S(C1-C8)алкила, S(галоген(C1-C8)алкил), S(O)(C1-C8)алкила, S(O)(галоген(C1-C8)алкил), S(O)2(C1-C8)алкила, S(O)2(галоген(C1-C8)алкил), N(R14)(R15),
(2) замещенного (C1-C8)алкила, где указанный замещенный (C1-C8)алкил содержит один или несколько заместителей, выбранных из CN и NO2,
(3) замещенного галоген(C1-C8)алкила, где указанный замещенный галоген(C1-C8)алкил содержит один или несколько заместителей, выбранных из CN и NO2,
(4) замещенного (C1-C8)алкокси, где указанный замещенный (C1-C8)алкокси содержит один или несколько заместителей, выбранных из CN и NO2, и
(5) замещенного галоген(C1-C8)алкокси, где указанный замещенный галоген(C1-C8)алкокси содержит один или несколько заместителей, выбранных из CN и NO2;
(c) R3 выбран из
(1) H, F, Cl, Br, I, CN, NO2, (C1-C8)алкила, галоген(C1-C8)алкила, (C1-C8)алкокси, галоген(C1-C8)алкокси, S(C1-C8)алкила, S(галоген(C1-C8)алкил), S(O)(C1-C8)алкила, S(O)(галоген(C1-C8)алкил), S(O)2(C1-C8)алкила, S(O)2(галоген(C1-C8)алкил), N(R14)(R15),
(2) замещенного (C1-C8)алкила, где указанный замещенный (C1-C8)алкил содержит один или несколько заместителей, выбранных из CN и NO2,
(3) замещенного галоген(C1-C8)алкила, где указанный замещенный галоген(C1-C8)алкил содержит один или несколько заместителей, выбранных из CN и NO2,
(4) замещенного (C1-C8)алкокси, где указанный замещенный (C1-C8)алкокси содержит один или несколько заместителей, выбранных из CN и NO2, и
(5) замещенного галоген(C1-C8)алкокси, где указанный замещенный галоген(C1-C8)алкокси содержит один или несколько заместителей, выбранных из CN и NO2;
(d) R4 выбран из
(1) H, F, Cl, Br, I, CN, NO2, (C1-C8)алкила, галоген(C1-C8)алкила, (C1-C8)алкокси, галоген(C1-C8)алкокси, S(C1-C8)алкила, S(галоген(C1-C8)алкил), S(O)( C1-C8)алкила, S(O)(галоген(C1-C8)алкил), S(O)2(C1-C8)алкила, S(O)2(галоген(C1-C8)алкил), N(R14)(R15),
(2) замещенного (C1-C8)алкила, где указанный замещенный (C1-C8)алкил содержит один или несколько заместителей, выбранных из CN и NO2,
(3) замещенного галоген(C1-C8)алкила, где указанный замещенный галоген(C1-C8)алкил содержит один или несколько заместителей, выбранных из CN и NO2,
(4) замещенного (C1-C8)алкокси, где указанный замещенный (C1-C8)алкокси содержит один или несколько заместителей, выбранных из CN и NO2, и
(5) замещенного галоген(C1-C8)алкокси, где указанный замещенный галоген(C1-C8)алкокси содержит один или несколько заместителей, выбранных из CN и NO2;
(e) R5 выбран из
(1) H, F, Cl, Br, I, CN, NO2, (C1-C8)алкила, галоген(C1-C8)алкила, (C1-C8)алкокси, галоген(C1-C8)алкокси, S(C1-C8)алкила, S(галоген(C1-C8)алкил), S(O)(C1-C8)алкила, S(O)(галоген(C1-C8)алкил), S(O)2(C1-C8)алкила, S(O)2(галоген(C1-C8)алкил), N(R14)(R15),
(2) замещенного (C1-C8)алкила, где указанный замещенный (C1-C8)алкил содержит один или несколько заместителей, выбранных из CN и NO2,
(3) замещенного галоген(C1-C8)алкила, где указанный замещенный галоген(C1-C8)алкил содержит один или несколько заместителей, выбранных из CN и NO2,
(4) замещенного (C1-C8)алкокси, где указанный замещенный (C1-C8)алкокси содержит один или несколько заместителей, выбранных из CN и NO2, и
(5) замещенного галоген(C1-C8)алкокси, где указанный замещенный галоген(C1-C8)алкокси содержит один или несколько заместителей, выбранных из CN и NO2;
(f) R6 представляет собой (C1-C8)галогеналкил;
(g) R7 выбран из H, F, Cl, Br, I, OH, (C1-C8)алкокси и галоген(C1-C8)алкокси;
(h) R8 выбран из H, (C1-C8)алкила, галоген(C1-C8)алкила, OR14 и N(R14)(R15);
(i) R9 выбран из H, F, Cl, Br, I, (C1-C8)алкила, галоген(C1-C8)алкила, (C1-C8)алкокси, галоген(C1-C8)алкокси, OR14 и N(R14)(R15);
(j) R10 выбран из
(1) (u), H, F, Cl, Br, I, CN, NO2, (C1-C8)алкила, галоген(C1-C8)алкила, (C1-C8)алкокси, галоген(C1-C8)алкокси, цикло(C3-C6)алкила, S(C1-C8)алкила, S(галоген(C1-C8)алкил), S(O)(C1-C8)алкила, S(O)(галоген(C1-C8)алкил), S(O)2(C1-C8)алкила, S(O)2(галоген(C1-C8)алкил), NR14R15, C(=O)H, C(=O)N(R14)(R15), CN(R14)(R15)(=NOH), (C=O)O(C1-C8)алкила, (C=O)OH, гетероциклила, (C2-C8)алкенила, галоген(C2-C8)алкенила, (C2-C8)алкинила,
(2) замещенного (C1-C8)алкила, где указанный замещенный (C1-C8)алкил содержит один или несколько заместителей, выбранных из OH, (C1-C8)алкокси, S(C1-C8)алкила, S(O)(C1-C8)алкила, S(O)2(C1-C8)алкила, NR14R15, и
(3) замещенного галоген(C1-C8)алкила, где указанный замещенный галоген(C1-C8)алкил содержит один или несколько заместителей, выбранных из (C1-C8)алкокси, S(C1-C8)алкила, S(O)(C1-C8)алкила, S(O)2(C1-C8)алкила и N(R14)(R15);
(k) R11 выбран из (и), замещенного (C1-C8)алкила, C(=O)OH, C(=O)O(C1-C8)алкила, C(=O)(замещенный-(C1-C8)алкил), C(=O)O(замещенный (C1-C8)алкил), C(=O)N(R14)(R15), C(=O)гетероциклила, C(=O)(замещенный гетероциклил), C(=S)N(R14)(R15), C(=S)гетероциклила, C(=S)(замещенный гетероциклил), (C1-C8)алкилN(R11a)(C(=X11)R11b), N(11a)(11d), ON(11c)(11d), галоген(C1-C8)алкила, (C1-C8)алкила, (C1-C8)алкилN(H)(гетероциклил), (C1-C8)алкил(N(R15))(C=O)O(C1-C8)алкила, (C1-C8)алкил (R14)(R15), N(H)N(H)(гетероциклил), B(OH)2, (C1-C8)алкилN(R11a)(C(=X11)R14), (C1-C8)алкилN(R11a)(C(=X11)N(R14)(R15)), (C1-C8)aлкилN(R11a)(C(=X11)OR14), замещенного или незамещенного гетероциклила, C(=O)N(R14)(N(R16)(R17), C(=O)N(R14)(( C1-C8)алкилC(=O)N(R14)N(R14)(R15)), C(=O)N(R14)(( C1-C8)алкилC(=O)N(R14)(R15)), C(=S)N(R14)(( C1-C8)алкилC(=S)N(R14)(R15)), C(=S)N(R14)(( C1-C8)алкилC(=O)N(R14)(R15)), C(=O)N(R14)(( C1-C8)алкилC(=S)N(R14)(R15)), C(=O)N(R14)(( C1-C8)алкилC(=O)(R15),
(1) где каждый указанный замещенный (C1-C8)алкил содержит один или несколько заместителей, выбранных из F, Cl, Br, I, CN, NO2, арила, замещенного арила, гетероциклила, замещенного гетероциклила, где каждый указанный замещенный арил содержит один или несколько заместителей, выбранных из F, Cl, Br, I, CN, NO2, (C1-C8)алкила, галоген(C1-C8)алкила, (C1-C8)алкокси, галоген(C1-C8)алкокси, S(C1-C8)алкила, S(галоген(C1-C8)алкил), N((C1-C8)алкил)2 (где каждый (C1-C8)алкил выбран независимо) и оксо,
(2) где каждый указанный замещенный гетероциклил содержит один или несколько заместителей, выбранных из F, Cl, Br, I, CN, NO2, (C1-C8)алкила, галоген(C1-C8)алкила, (C1-C8)алкокси, галоген(C1-C8)алкокси, S(C1-C8)алкила, S(галоген(C1-C8)алкил), N((C1-C8)алкил)2 (где каждый (C1-C8)алкил выбран независимо), C(=O)(C1-C8)алкила, C(=O)(C3-C6)циклоалкила, S(=O)2(C1-C8)алкила, NR14R15 и оксо,
(3) где R11a выбран из H, (C1-C8)алкила и (C1-C8)алкилгетероциклила, R14, C(X11)R14, (C1-C8)aлкилR14,
(4) где R11b выбран из (С1-С8)алкила, цикло(C3-C6)алкила, галоген(C1-C8)алкила, гетероциклила, замещенного гетероциклила (где указанные заместители представляют собой один или несколько из F, Cl, Br, I, CN, NO2, (C1-C8)алкила, галоген(C1-C8)алкила, (C1-C8)алкокси, галоген(C1-C8)алкокси, S(C1-C8)алкила, S(галоген(C1-C8)алкил), N((C1-C8)алкил)2 (где каждый (C1-C8)алкил выбран независимо) и оксо), (C1-C8)алкилS(C1-C8)алкила, (C1-C8)алкилS(O)(C1-C8)алкила, (C1-C8)алкилS(O)2(C1-C8)алкила, N(R11c)(R11d), O(C1-C8)алкила, O-гетероциклила, O-замещенного гетероциклила (где указанные заместители представляют собой один или несколько из F, Cl, Br, I, CN, NO2, (C1-C8)алкила, галоген(C1-C8)алкила, (C1-C8)алкокси, галоген(C1-C8)алкокси, S(C1-C8)алкила, S(галоген(C1-C8)алкил), N((C1-C8)алкил)2 (где каждый (C1-C8)алкил выбран независимо) и оксо), C(=O)OR11d, C(=O)N(R11c)(R11d), C(=O)(R11d)арила, замещенного арила (где указанные заместители представляют собой один или несколько из F, Cl, Br, I, CN, NO2, (C1-C8)алкила, галоген(C1-C8)алкила, (C1-C8)алкокси, галоген(C1-C8)алкокси, S(C1-C8)алкила, S(галоген(C1-C8)алкил), N((C1-C8)алкил)2 (где каждый (C1-C8)алкил выбран независимо),
(5) где X11 представляет собой O или S,
(6) где R11c выбран из H,
(7) где R11d выбран из H, (C1-C8)алкила, (C1-C8)алкенила, галоген(C1-C8)алкила, гетероциклила, замещенного гетероциклила (где указанные заместители представляют собой один или несколько из F, Cl, Br, I, CN, NO2, (C1-C8)алкила, галоген(C1-C8)алкила, (C1-C8)алкокси, галоген(C1-C8)алкокси, S(C1-C8)алкила, S(галоген(C1-C8)алкил), N((C1-C8)алкил)2 (где каждый (C1-C8)алкил выбран независимо) и оксо), N(H)(C(=O)цикло(C3-C6)алкил), N(H)(C(=O)галоген(C1-C8)алкил),
(8) где необязательно R11c и R11d вместе с N образуют 5-, 6-, 7- или 8-членное кольцо, которое необязательно может дополнительно содержать 1, 2 или 3 дополнительных гетероатома, выбранных из O, N или S, в кольце;
(l) R12 выбран из (v), H, F, Cl, Br, I, CN, (C1-C8)алкила, галоген(C1-C8)алкила, (C1-C8)алкокси, галоген(C1-C8)алкокси и цикло(C3-C6)алкила;
(m) R13 выбран из (v), H, F, Cl, Br, I, CN, (C1-C8)алкила, галоген(C1-C8)алкила, (C1-C8)алкокси и галоген(C1-C8)алкокси;
(n) каждый R14 выбран независимо из H, (C1-C8)алкила, (C1-C8)алкенила, замещенного (C1-C8)алкила, галоген(C1-C8)алкила, замещенного галоген(C1-C8)алкила, (C1-C8)алкокси, цикло(C3-C6)алкила, арила, замещенного арила, (C1-C8)алкиларила, (C1-C8)алкил-(замещенный арил), O-(C1-C8)алкиларила, O-(C1-C8)алкил-(замещенный арил), гетероциклила, замещенного гетероциклила, (C1-C8)алкилгетероциклила, (C1-C8)алкил-(замещенный гетероциклил), O-(C1-C8)алкилгетероциклила, O-(C1-C8)алкил-(замещенный гетероциклил), N(R16)(R17), (C1-C8)алкил-C(=O)N(R16)(R17), C(=O)( C1-C8)алкила, C(=O)(галоген(C1-C8)алкил), C(=O)(C3-C6)циклоалкила, (C1-C8)алкил-C(=O)O(C1-C8)алкила, C(=O)H,
где каждый указанный замещенный (C1-C8)алкил содержит один или несколько заместителей, выбранных из CN и NO2,
где каждый указанный замещенный галоген(C1-C8)алкил содержит один или несколько заместителей, выбранных из CN и NO2,
где каждый указанный замещенный арил содержит один или несколько заместителей, выбранных из F, Cl, Br, I, CN, NO2, (C1-C8)алкила, галоген(C1-C8)алкила, (C1-C8)алкокси, галоген(C1-C8)алкокси, S(C1-C8)алкила, S(галоген(C1-C8)алкил), N((C1-C8)алкил)2 (где каждый (C1-C8)алкил выбран независимо) и оксо и
где каждый указанный замещенный гетероциклил содержит один или несколько заместителей, выбранных из F, Cl, Br, I, CN, NO2, (C1-C8)алкила, галоген(C1-C8)алкила, (C1-C8)алкокси, галоген(C1-C8)алкокси, (C3-C6)циклоалкил S(C1-C8)алкила, S(галоген(C1-C8)алкил), N((C1-C8)алкил)2 (где каждый (C1-C8)алкил выбран независимо), гетероциклила, C(=O)(C1-C8)алкила, C(=O)O(C1-C8)алкила и оксо (где указанный алкил, алкокси и гетероциклил может быть дополнительно замещен одним или несколькими из F, Cl, Br, I, CN и NO2);
(o) каждый R15 выбран независимо из H, (C1-C8)алкила, (C1-C8)алкенила, замещенного (C1-C8)алкила, галоген(C1-C8)алкила, замещенного галоген(C1-C8)алкила, (C1-C8)алкокси, цикло(C3-C6)алкила, арила, замещенного арила, (C1-C8)алкиларила, (C1-C8)алкил-(замещенный арил), O-(C1-C8)алкиларила, O-(C1-C8)алкил-(замещенный арил), гетероциклила, замещенного гетероциклила, (C1-C8)алкилгетероциклила, (C1-C8)алкил-(замещенный гетероциклил), O-( C1-C8)алкилгетероциклила, O-(C1-C8)алкил-(замещенный гетероциклил), N(R16)(R17), (C1-C8)алкил-C(=O)N(R16)(R17), C(=O)( C1-C8)алкила, C(=O)(галоген(C1-C8)алкил), C(=O)(C3-C6)циклоалкила, (C1-C8)алкил-C(=O)O(C1-C8)алкила, C(=O)H
где каждый указанный замещенный (С1-С8)алкил содержит один или несколько заместителей, выбранных из CN и NO2,
где каждый указанный замещенный галоген(C1-C8)алкил содержит один или несколько заместителей, выбранных из CN и NO2,
где каждый указанный замещенный арил содержит один или несколько заместителей, выбранных из F, Cl, Br, I, CN, NO2, (C1-C8)алкила, галоген(C1-C8)алкила, (C1-C8)алкокси, галоген(C1-C8)алкокси, S(C1-C8)алкила, S(галоген(C1-C8)алкил), N((C1-C8)алкил)2 (где каждый (C1-C8)алкил выбран независимо) и оксо и
где каждый указанный замещенный гетероциклил содержит один или несколько заместителей, выбранных из F, Cl, Br, I, CN, NO2, (C1-C8)алкила, галоген(C1-C8)алкила, (C1-C8)алкокси, галоген(C1-C8)алкокси, (C3-C6)циклоалкил S(C1-C8)алкила, S(галоген(C1-C8)алкил), N((C1-C8)алкил)2 (где каждый (C1-C8)алкил выбран независимо), гетероциклила, C(=O)(C1-C8)алкила, C(=O)O(C1-C8)алкила и оксо (где указанный алкил, алкокси и гетероциклил, может быть дополнительно замещен одним или несколькими из F, Cl, Br, I, CN и NO2);
(p) каждый R16 выбран независимо из H, (C1-C8)алкила, замещенного-(C1-C8)алкила, галоген(C1-C8)алкила, замещенный-галоген(C1-C8)алкила, цикло(C3-C6)алкила, арила, замещенного арила, (C1-C8)алкиларила, (C1-C8)алкил-(замещенный арил), O-(C1-C8)алкиларила, O-(C1-C8)алкил-(замещенный арил), гетероциклила, замещенного гетероциклила, (C1-C8)алкилгетероциклила, (C1-C8)алкил-(замещенный гетероциклил), O-(C1-C8)алкилгетероциклила, O-(C1-C8)алкил-(замещенный гетероциклил), O-(C1-C8)алкила,
где каждый указанный замещенный (C1-C8)алкил содержит один или несколько заместителей, выбранных из CN и NO2,
где каждый указанный замещенный галоген(C1-C8)алкил содержит один или несколько заместителей, выбранных из CN и NO2,
где каждый указанный замещенный арил содержит один или несколько заместителей, выбранных из F, Cl, Br, I, CN, NO2, (C1-C8)алкила, галоген(C1-C8)алкила, (C1-C8)алкокси, галоген(C1-C8)алкокси, S(C1-C8)алкила, S(галоген(C1-C8)алкил), N((C1-C8)алкил)2 (где каждый (C1-C8)алкил выбран независимо) и оксо и
где каждый указанный замещенный гетероциклил содержит один или несколько заместителей, выбранных из F, Cl, Br, I, CN, NO2, (C1-C8)алкила, галоген(C1-C8)алкила, (C1-C8)алкокси, галоген(C1-C8)алкокси, S(C1-C8)алкила, S(галоген(C1-C8)алкил), N((C1-C8)алкил)2 (где каждый (C1-C8)алкил выбран независимо) и оксо;
(q) каждый R17 выбран независимо из H, (C1-C8)алкила, замещенного-(C1-C8)алкила, галоген(C1-C8)алкила, замещенный-галоген(C1-C8)алкила, цикло(C3-C6)алкила, арила, замещенного арила, (C1-C8)алкиларила, (C1-C8)алкил-(замещенный арил), O-(C1-C8)алкиларила, O-(C1-C8)алкил-(замещенный арил), гетероциклила, замещенного гетероциклила, (C1-C8)алкилгетероциклила, (C1-C8)алкил-(замещенный гетероциклил), O-(C1-C8)алкилгетероциклила, O-(C1-C8)алкил-(замещенный гетероциклил), O-(C1-C8)алкила,
где каждый указанный замещенный (C1-C8)алкил содержит один или несколько заместителей, выбранных из CN и NO2,
где каждый указанный замещенный галоген(C1-C8)алкил содержит один или несколько заместителей, выбранных из CN и NO2,
где каждый указанный замещенный арил содержит один или несколько заместителей, выбранных из F, Cl, Br, I, CN, NO2, (C1-C8)алкила, галоген(C1-C8)алкила, (C1-C8)алкокси, галоген(C1-C8)алкокси, S(C1-C8)алкила, S(галоген(C1-C8)алкил), N((C1-C8)алкил)2 (где каждый (C1-C8)алкил выбран независимо) и оксо и
где каждый указанный замещенный гетероциклил содержит один или несколько заместителей, выбранных из F, Cl, Br, I, CN, NO2, (C1-C8)алкила, галоген(C1-C8)алкила, (C1-C8)алкокси, галоген(C1-C8)алкокси, S(C1-C8)алкила, S(галоген(C1-C8)алкил), N((C1-C8)алкил)2 (где каждый (C1-C8)алкил выбран независимо) и оксо;
(r) X1 выбран из N и CR12;
(s) X2 выбран из N, CR9 и CR13;
(t) X3 выбран из N и CR9;
(u) R10 и R11 вместе образуют связь, содержащую 3-4 атома, выбранных из C, N, O и S, где указанная связь присоединяется обратно к кольцу с образованием 5-6-членного насыщенного или ненасыщенного циклического кольца, где указанная связь содержит по меньшей мере один заместитель X4, где X4 выбран из F, Cl, Br, I, R14, N(R14)(R15), N(R14)(C(=O)R14), N(R14)(C(=S)R14), N(R14)(C(=O)N(R14)(R14)), N(R14)(C(=S)N(R14)(R14)), N(R14)(C(=O)N(R14)((C1-C8)алкенил)), N(R14)(C(=S)N(R14)((C1-C8)алкенил)), оксо, C(=O)(C1-C8)алкилN(R14)(R14), (C1-C8)алкилC(=O)N(R14)R(15), где каждый R14 выбран независимо;
(v) R12 и R13 вместе образуют связь, содержащую 3-4 атома, выбранных из C, N, O и S, где указанная связь присоединяется обратно к кольцу с образованием 5-6-членного насыщенного или ненасыщенного циклического кольца, где указанная связь содержит по меньшей мере один заместитель X4, где X4 выбран из R14, N(R14)(R15), N(R14)(C(=O)R14), N(R14)(C(=S)R14), N(R14)(C(=O)N(R14)(R14)), N(R14)(C(=S)N(R14)(R14)), N(R14)(C(=O)N(R14)((C1-C8)алкенил)), N(R14)(C(=S)N(R14)((C1-C8)алкенил)), где каждый R14 выбран независимо.
2. Молекула по п.1, где R1 выбран из H, F, Cl, Br, I, CN, NO2, метила, этила, (C3)алкила, (C4)алкила, (C5)алкила, (C6)алкила, (C7)алкила, (C8)алкила, галогенметила, галогенэтила, галоген(C3)алкила, галоген(C4)алкила, галоген(C5)алкила, галоген(C6)алкила, галоген(C7)алкила, галоген(C8)алкила, метокси, этокси, (C3)алкокси, (C4)алкокси, (C5)алкокси, (C6)алкокси, (C7)алкокси, (C8)алкокси, галогенметокси, галогенэтокси, галоген(C3)алкокси, галоген(C4)алкокси, галоген(C5)алкокси, галоген(C6)алкокси, галоген(C7)алкокси и галоген(C8)алкокси, предпочтительно из Cl и H,
R2 выбран из H, F, Cl, Br, I, CN, NO2, метила, этила, (C3)алкила, (C4)алкила, (C5)алкила, (C6)алкила, (C7)алкила, (C8)алкила, галогенметила, галогенэтила, галоген(C3)алкила, галоген(C4)алкила, галоген(C5)алкила, галоген(C6)алкила, галоген(C7)алкила, галоген(C8)алкила, метокси, этокси, (C3)алкокси, (C4)алкокси, (C5)алкокси, (C6)алкокси, (C7)алкокси, (C8)алкокси, галогенметокси, галогенэтокси, галоген(C3)алкокси, галоген(C4)алкокси, галоген(C5)алкокси, галоген(C6)алкокси, галоген(C7)алкокси и галоген(C8)алкокси, предпочтительно из CF3, CH3, Cl, F и H,
R3 выбран из H, F, Cl, Br, I, CN, NO2, метила, этила, (C3)алкила, (C4)алкила, (C5)алкила, (C6)алкила, (C7)алкила, (C8)алкила, галогенметила, галогенэтила, галоген(C3)алкила, галоген(C4)алкила, галоген(C5)алкила, галоген(C6)алкила, галоген(C7)алкила, галоген(C8)алкила, метокси, этокси, (C3)алкокси, (C4)алкокси, (C5)алкокси, (C6)алкокси, (C7)алкокси, (C8)алкокси, галогенметокси, галогенэтокси, галоген(C3)алкокси, галоген(C4)алкокси, галоген(C5)алкокси, галоген(C6)алкокси, галоген(C7)алкокси и галоген(C8)алкокси, предпочтительно из OCH3, CH3, F, Cl или H,
R4 выбран из H, F, Cl, Br, I, CN, NO2, метила, этила, (C3)алкила, (C4)алкила, (C5)алкила, (C6)алкила, (C7)алкила, (C8)алкила, галогенметила, галогенэтила, галоген(C3)алкила, галоген(C4)алкила, галоген(C5)алкила, галоген(C6)алкила, галоген(C7)алкила, галоген(C8)алкила, метокси, этокси, (C3)алкокси, (C4)алкокси, (C5)алкокси, (C6)алкокси, (C7)алкокси, (C8)алкокси, галогенметокси, галогенэтокси, галоген(C3)алкокси, галоген(C4)алкокси, галоген(C5)алкокси, галоген(C6)алкокси, галоген(C7)алкокси и галоген(C8)алкокси, предпочтительно из CF3, CH3, Cl, F и H,
R5 выбран из H, F, Cl, Br, I, CN, NO2, метила, этила, (C3)алкила, (C4)алкила, (C5)алкила, (C6)алкила, (C7)алкила, (C8)алкила, галогенметила, галогенэтила, галоген(C3)алкила, галоген(C4)алкила, галоген(C5)алкила, галоген(C6)алкила, галоген(C7)алкила, галоген(C8)алкила, метокси, этокси, (C3)алкокси, (C4)алкокси, (C5)алкокси, (C6)алкокси, (C7)алкокси, (C8)алкокси, галогенметокси, галогенэтокси, галоген(C3)алкокси, галоген(C4)алкокси, галоген(C5)алкокси, галоген(C6)алкокси, галоген(C7)алкокси и галоген(C8)алкокси, предпочтительно из F, Cl и H,
R2 и R4 выбраны из F, Cl, Br, I, CN и NO2, и R1, R3 и R5 представляют собой H,
R2, R3 и R4 выбраны из F, Cl, Br, I, CN и NO2, и R1 и R5 представляют собой H, предпочтительно
где R2, R3 и R4 независимо выбраны из F и Cl, и R1 и R5 представляют собой H,
R6 выбран из галогенметила, галогенэтила, галоген(C3)алкила, галоген(C4)алкила, галоген(C5)алкила, галоген(C6)алкила, галоген(C7)алкила и галоген(C8)алкила, и предпочтительно
представляет собой трифторметил,
R7 выбран из H, F, Cl, Br, I, OCH3 и OH,
R8 выбран из H, метила, этила, (C3)алкила, (C4)алкила, (C5)алкила, (C6)алкила, (C7)алкила, (C8)алкила, галогенметила, галогенэтила, галоген(C3)алкила, галоген(C4)алкила, галоген(C5)алкила, галоген(C6)алкила, галоген(C7)алкила и галоген(C8)алкила, предпочтительно из CH3 и H,
R9 выбран из H, F, Cl, Br, I, метила, этила, (C3)алкила, (C4)алкила, (C5)алкила, (C6)алкила, (C7)алкила, (C8)алкила, галогенметила, галогенэтила, галоген(C3)алкила, галоген(C4)алкила, галоген(C5)алкила, галоген(C6)алкила, галоген(C7)алкила, галоген(C8)алкила, метокси, этокси, (C3)алкокси, (C4)алкокси, (C5)алкокси, (C6)алкокси, (C7)алкокси, (C8)алкокси, галогенметокси, галогенэтокси, галоген(C3)алкокси, галоген(C4)алкокси, галоген(C5)алкокси, галоген(C6)алкокси, галоген(C7)алкокси и галоген(C8)алкокси,
R10 выбран из Br, C(=NOH)NH2, C(=O)H, C(=O)NH2, C(=O)OCH2CH3, C(=O)OH, CF3, CH2CH3, CH2OH, CH3, Cl, CN, F, H, NH2, NHC(=O)H, NHCH3, NO2, OCH3, OCHF2 и пиридила или из H, F, Cl, Br, I, CN, метила, этила, (C3)алкила, (C4)алкила, (C5)алкила, (C6)алкила, (C7)алкила, (C8)алкила, галогенметила, галогенэтила, галоген(C3)алкила, галоген(C4)алкила, галоген(C5)алкила, галоген(C6)алкила, галоген(C7)алкила, галоген(C8)алкила, метокси, этокси, (C3)алкокси, (C4)алкокси, (C5)алкокси, (C6)алкокси, (C7)алкокси, (C8)алкокси, галогенметокси, галогенэтокси, галоген(C3)алкокси, галоген(C4)алкокси, галоген(C5)алкокси, галоген(C6)алкокси, галоген(C7)алкокси, галоген(C8)алкокси, циклопропила, циклобутила, циклопентила и циклогексила, предпочтительно из H, Cl, Br, CH3 и CF3,
R11 выбран из C(=O)(замещенный-(C1-C8)алкил), C(=O)N(R14)(R15), C(=O)гетероциклила и C(=O)(замещенный гетероциклил), и предпочтительно C(=O)морфолинил, или выбран из CH2N(H)C(=O)CH3, CH2N(H)C(=O)циклопропила, CH2N(H)C(=O)CH2CF3, CH2N(H)C(=O)CH2CH3, CH2N(H)C(=O)C(CH3)3, CH2N(H)C(=O)(хлорпиридил), CH2N(H)C(=O)CH2(хлорпиридил), CH2N(H)C(=O)CH2CH2SCH3, N(H)C(=O)(пиридил), CH2N(CH2пиридил)C(=O)циклопропила, CH2N(H)C(=O)N(H)(CH2CH3), CH2N(H)C(=O)морфолинила, CH2N(H)C(=O)N(H)(пиридил), CH2N(H)C(=O)NH2, CH2N(H)C(=O)NH(CH2CH3), CH2N(H)C(=O)NH(CH2CHCH2), CH2N(H)C(=O)OC(CH3)3, CH2N(H)C(=O)O(хлорфенил), CH2N(H)C(=O)(C=O)OCH3, CH2N(H)C(=O)(C=O)N(H)CH2CF3, CH2N(H)(пиридил), N(H)N(H)C(=O)циклопропила, N(H)N(H)C(=O)CH2CF3, ON(H)C(=O)циклопропила и ON(H)C(=O)CH2CF3, или из 1,2,4-триазолила, 1,2,4-триазолил-C(=O)циклопропила, 1,2,4-триазолил-C(=O)CH3, 1,2-метилтриазолила, 1,2,4-триазолил-H(C(=O)циклопропил)2, 1,2,4-триазолилN(H)(C(=O)циклопропил), 1,2,4-триазолилNH2, 1,2,4-триазолил-NO2, 1,2,4-триазолилS(O)2CH3, 1,2,4-триазолилSCH3, C(=O)(морфолинил), C(=O)N(CH3)(CH3), C(=O)N(H)(CH(CH3)хлорпиридинил), C(=O)N(H)(CH2C(=O)N(CH3)(CH2CF3)), C(=O)N(H)(CH2-бензотиазолил), C(=O)N(H)(CH2C(=O)N(H)(CH2CF3)), C(=O)N(H)(CH2C(=O)N(H)(CH2CH=CH2)), C(=O)N(H)(CH2C(=O)N(H)(циклопропил)), C(=O)N(H)(CH2C(=O)N(H)(N(CH3)2)), C(=O)N(H)(CH2C(=O)N(H)(OCH3)), C(=O)N(H)(CH2C(=O)N(H)(тиэтанил)), C(=O)N(H)(CH2C(=O)N(H)(диоксид тиэтанила)), C(=O)N(H)(CH2C(=O)OC(CH3)3), C(=O)N(H)(CH2C(=S)N(H)(CH2CF3)), C(=O)N(H)(CH2CF3), C(=O)N(H)(CH2CH2-хлорпиридинил), C(=O)N(H)(CH2-фуранил), C(=O)N(H)(CH2-метилимидазолил), C(=O)N(H)(CH2-циклопропилоксадиазолил), C(=O)N(H)(CH2-фенил), C(=O)N(H)(CH2-трифторметилфенил), C(=O)N(H)(CH2-фторфенил), C(=O)N(H)(CH2-пиразинил), C(=O)N(H)(CH2-трифторметилпиридинил), C(=O)N(H)(CH2-хлорпиридинил), C(=O)N(H)(CH2-пиридинил-NO2), C(=O)N(H)(CH2-пиридинил-OCH3), C(=O)N(H)(CH2-пиримидинил), C(=O)N(H)(CH2-тетрагидрофуранил), C(=О)N(H)(CH2-хлортиазолил), C(=O)N(H)(CH3), C(=O)NH2, C(=O)N(H)(N(CH3)(фторфенил)), C(=O)N(H)(N(H)(фторфенил)), C(=O)N(H)(OCH2-хлорпиридинил), C(=O)N(H)(пиперидинил), C(=O)N(H)(пиперидинилC(=O)CH2CF3), C(=O)N(H)(пиперидинил-CH2CN), C(=O)N(H)(пиперидинилC(=O)CH3), C(=O)N(H)(пиперидинилCH2CH2OH), C(=O)N(H)(пиперидинилоксэтанил), C(=O)N(H)(хлорпиридинил), C(=O)N(H)(CH2-тетрагидропиранил), C(=O)N(H)(тиэтанил), C(=O)N(H)(диоксид тиэтанила), C(=O)N(H)(оксид тиэтанила), C(=O)N(H)(CH2-пиразинил), C(=O)пирролидинилоксо, C(=S)N(H)(CH2C(=O)N(H)(CH2CF3)), C(=S)N(H)(CH2C(=S)N(H)(CH2CF3)), C(=S)N(H)(CH2-хлорпиридинил), CH2N(CH2-пиридинил)(C(=O)-циклопропил), CH2N(H)(C(=O)C(=O)N(H)(CH2CF3), CH2N(H)(C(=O)C(=O)OCH3), CH2N(H)(C(=O)C(CH3)3), CH2N(H)(C(=O)-CH2-хлорпиридинил), CH2N(H)(C(=O)CH2CF3), CH2N(H)(C(=O)CH2CH2S(O)2CH3), CH2N(H)(C(=O)CH2CH2SCH3), CH2N(H)(C(=O)CH2CH3), CH2N(H)(C(=O)-циклопропил), CH2N(Н)(С(=O)морфолинил), CH2N(H)(C(=O)N(CH3)2, CH2N(H)(C(=O)N(H)(CH2CH3)), CH2N(H)(C(=О)N(H)(пиридинил)), CH2N(H)(C(=O)OC(CH3)3), CH2N(H)(C(=O)O-хлорфенил), CH2N(H)(C(=O)-пиридинил), CH2N(H)(C(=O)-хлорпиридинил), CH2N(H)(C(=S)циклопропил), CH2N(H)(C(=S)N(H)(CH2CH=CH2)), CH2N(H)(C(=S)N(H)(CH2CH3)), CH2N(H)(пиридинил), N(H)(N(H)(C(=O)CH2CF3), N(H)(N(H)(C(=O)циклопропил), ON(H)(C(=O)CH2CF3) и ON(H)(C(=O)циклопропил),
R12 выбран из H, F, Cl, Br, I, метила, этила, (C3)алкила, (C4)алкила, (C5)алкила, (C6)алкила, (C7)алкила, (C8)алкила, галогенметила, галогенэтила, галоген(C3)алкила, галоген(C4)алкила, галоген(C5)алкила, галоген(C6)алкила, галоген(C7)алкила, галоген(C8)алкила, галогенметокси, галогенэтокси, галоген(C3)алкокси, галоген(C4)алкокси, галоген(C5)алкокси, галоген(C6)алкокси, галоген(C7)алкокси и галоген(C8)алкокси, предпочтительно из CH3 и H,
R13 выбран из H, F, Cl, Br, I, метила, этила, (C3)алкила, (C4)алкила, (C5)алкила, (C6)алкила, (C7)алкила, (C8)алкила, галогенметила, галогенэтила, галоген(C3)алкила, галоген(C4)алкила, галоген(C5)алкила, галоген(C6)алкила, галоген(C7)алкила, галоген(C8)алкила, галогенметокси, галогенэтокси, галоген(C3)алкокси, галоген(C4)алкокси, галоген(C5)алкокси, галоген(C6)алкокси, галоген(C7)алкокси и галоген(C8)алкокси, предпочтительно из CH3, Cl и H,
R12-R13 представляет собой гидрокарбильную связь CH=CHCH=CH,
R14 и R15 независимо выбраны из H, метила, этила, (C3)алкила, (C4)алкила, (C5)алкила, (C6)алкила, (C7)алкила, (C8)алкила, галогенметила, галогенэтила, галоген(C3)алкила, галоген(C4)алкила, галоген(C5)алкила, галоген(C6)алкила, галоген(C7)алкила, галоген(C8)алкила, метиларила, этиларила, (C3)алкиларила, (C4)алкиларила, (C5)алкиларила, (C6)алкиларила, (C7)алкиларила, (C8)алкиларила, метил-(замещенный арил), этил-(замещенный арил), (C3)алкил-(замещенный арил), (C4)алкил-(замещенный арил), (C5)алкил-(замещенный арил), (C6)алкил-(замещенный арил), (C7)алкил-(замещенный арил), (C8)алкил-(замещенный арил), O-метиларила, O-этиларила, O-(C3)алкиларила, O-(C4)алкиларила, O-(C5)алкиларила, O-(C6)алкиларила, O-(C7)алкиларила, O-(C8)алкиларила, O-метил-(замещенный арил), O-этил-(замещенный арил), O-(C3)алкил-(замещенный арил), O-(C4)алкил-(замещенный арил), O-(C5)алкил-(замещенный арил), O-(C6)алкил-(замещенный арил), O-(C7)алкил-(замещенный арил), O-(C8)алкил-(замещенный арил), метилгетероциклила, этилгетероциклила, (C3)алкилгетероциклила, (C4)алкилгетероциклила, (C5)алкилгетероциклила, (C6)алкилгетероциклила, (C7)алкилгетероциклила, (C8)алкилгетероциклила, метил-(замещенный гетероциклил), этил-(замещенный гетероциклил), (C3)алкил-(замещенный гетероциклил), (C4)алкил-(замещенный гетероциклил), (C5)алкил-(замещенный гетероциклил), (C6)алкил-(замещенный гетероциклил), (C7)алкил-(замещенный гетероциклил), (C8)алкил-(замещенный гетероциклил), O-метилгетероциклила, O-этилгетероциклила, O-(C3)алкилгетероциклила, O-(C4)алкилгетероциклила, O-(C5)алкилгетероциклила, O-(C6)алкилгетероциклила, O-(C7)алкилгетероциклила, O-(C8)алкилгетероциклила, O-метил-(замещенный гетероциклил), O-этил-(замещенный гетероциклил), O-(C3)алкил-(замещенный гетероциклил), O-(C4)алкил-(замещенный гетероциклил), O-(C5)алкил-(замещенный гетероциклил), O-(C6)алкил-(замещенный гетероциклил), O-(C7)алкил-(замещенный гетероциклил), O-(C8)алкил-(замещенный гетероциклил), метил-C(=O)N(R16)(R17), этил-C(=O)N(R16)(R17), (C3)алкил-C(=O)N(R16)(R17), (C4)алкил-C(=O)N(R16)(R17), (C5)алкил-C(=O)N(R16)(R17), (C6)алкил-C(=O)N(R16)(R17), (C7)алкил-C(=O)N(R16)(R17) и (C8)алкил-C(=O)N(R16)(R17), или из H, CH3, CH2CF3, CH2-галогенпиридила, оксопирролидинила, галогенфенила, тиэтанила, CH2-фенила, CH2-пиридила, диоксида тиэтанила, CH2-галогентиазолила, C((CH3)2)-пиридила, N(H)(галогенфенил), CH2-пиримидинила, CH2-тетрагидрофуранила, CH2-фуранила, O-CH2-галогенпиридила и CH2C(=O)N(H)(CH2CF3),
R16 и R17 независимо выбраны из H, метила, этила, (C3)алкила, (C4)алкила, (C5)алкила, (C6)алкила, (C7)алкила, (C8)алкила, галогенметила, галогенэтила, галоген(C3)алкила, галоген(C4)алкила, галоген(C5)алкила, галоген(C6)алкила, галоген(C7)алкила, галоген(C8)алкила, метиларила, этиларила, (C3)алкиларила, (C4)алкиларила, (C5)алкиларила, (C6)алкиларила, (C7)алкиларила, (C8)алкиларила, метил-(замещенный арил), этил-(замещенный арил), (C3)алкил-(замещенный арил), (C4)алкил-(замещенный арил), (C5)алкил-(замещенный арил), (C6)алкил-(замещенный арил), (C7)алкил-(замещенный арил), (C8)алкил-(замещенный арил), O-метиларила, O-этиларила, O-(C3)алкиларила, O-(C4)алкиларила, O-(C5)алкиларила, O-(C6)алкиларила, O-(C7)алкиларила, O-(C8)алкиларила, O-метил-(замещенный арил), O-этил-(замещенный арил), O-(C3)алкил-(замещенный арил), O-(C4)алкил-(замещенный арил), O-(C5)алкил-(замещенный арил), O-(C6)алкил-(замещенный арил), O-(C7)алкил-(замещенный арил), O-(C8)алкил-(замещенный арил), метилгетероциклила, этилгетероциклила, (C3)алкилгетероциклила, (C4)алкилгетероциклила, (C5)алкилгетероциклила, (C6)алкилгетероциклила, (C7)алкилгетероциклила, (C8)алкилгетероциклила, метил-(замещенный гетероциклил), этил-(замещенный гетероциклил), (C3)алкил-(замещенный гетероциклил), (C4)алкил-(замещенный гетероциклил), (C5)алкил-(замещенный гетероциклил), (C6)алкил-(замещенный гетероциклил), (C7)алкил-(замещенный гетероциклил), (C8)алкил-(замещенный гетероциклил), O-метилгетероциклила, O-этилгетероциклила, O-(C3)алкилгетероциклила, O-(C4)алкилгетероциклила, O-(C5)алкилгетероциклила, O-(C6)алкилгетероциклила, O-(C7)алкилгетероциклила, O-(C8)алкилгетероциклила, O-метил-(замещенный гетероциклил), O-этил-(замещенный гетероциклил), O-(C3)алкил-(замещенный гетероциклил), O-(C4)алкил-(замещенный гетероциклил), O-(C5)алкил-(замещенный гетероциклил), O-(C6)алкил-(замещенный гетероциклил), O-(C7)алкил-(замещенный гетероциклил) и O-(C8)алкил-(замещенный гетероциклил), или из H, CH2CF3, циклопропила, тиэтанила, диоксида тиэтанила и галогенфенила,
X1 представляет собой CR12, X2 представляет собой CR13 и X3 представляет собой CR9, или
R10 и R11 образуют связь, и указанная связь выбрана из (a)-(l)
где "∗" обозначает присоединение обратно к кольцу (Отмечено, что поскольку структуры изображены таким образом, они могут быть зеркально отражены снизу вверх, тем самым вращая структуру на 180 градусов) (отмечено, что атомы водорода для атомов углерода подразумеваются и не показаны).
4. Композиция по п.1, дополнительно содержащая:
I.
(a) одно или несколько соединений, характеризующихся акарицидными, альгицидными, авицидными, бактерицидными, фунгицидными, гербицидными, инсектицидными, моллюскоцидными, нематоцидными, родентицидными или вироцидными свойствами; или
(b) одно или несколько соединений, которые представляют собой антифиданты, средства для отпугивания птиц, хемостерилизаторы, антидоты, приманки для насекомых, средства для отпугивания насекомых, средства для отпугивания млекопитающих, средства дезориентации самцов, активаторы растений, регуляторы роста растений или синергисты; или
(c) оба (a) и (b);
II.
одно или несколько соединений, выбранных из: бромида (3-этоксипропил)ртути, 1,2-дихлорпропана, 1,3-дихлорпропена, 1-метилциклопропена, 1-нафтола, 2-(октилтио)этанола, 2,3,5-три-йодбензойной кислоты, 2,3,6-TBA, 2,3,6-TBA-диметиламмония, 2,3,6-TBA-лития, 2,3,6-TBA-калия, 2,3,6-TBA-натрия, 2,4,5-T, 2,4,5-T-2-бутоксипропила, 2,4,5-T-2-этилгексила, 2,4,5-T-3-бутоксипропила, 2,4,5-TB, 2,4,5-T-бутометила, 2,4,5-T-бутотила, 2,4,5-T-бутила, 2,4,5-T-изобутила, 2,4,5-T-изооктила, 2,4,5-T-изопропила, 2,4,5-T-метила, 2,4,5-T-пентила, 2,4,5-T-натрия, 2,4,5-T-триэтиламмония, 2,4,5-T-троламина, 2,4-D, 2,4-D-2-бутоксипропила, 2,4-D-2-этилгексила, 2,4-D-3-бутоксипропила, 2,4-D-аммония, 2,4-DB, 2,4-DB-бутила, 2,4-DB-диметиламмония, 2,4-DB-изооктила, 2,4-DB-калия, 2,4-DB-натрия, 2,4-D-бутотила, 2,4-D-бутила, 2,4-D-диэтиламмония, 2,4-D-диметиламмония, 2,4-D-диоламина, 2,4-D-додециламмония, 2,4-DEB, 2,4-DEP, 2,4-D-этила, 2,4-D-гептиламмония, 2,4-D-изобутила, 2,4-D-изооктила, 2,4-D-изопропила, 2,4-D-изопропиламмония, 2,4-D-лития, 2,4-D-мептила, 2,4-D-метила, 2,4-D-октила, 2,4-D-пентила, 2,4-D-калия, 2,4-D-пропила, 2,4-D-натрия, 2,4-D-тефурила, 2,4-D-тетрадециламмония, 2,4-D-триэтиламмония, 2,4-D-трис(2-гидроксипропил)аммония, 2,4-D-троламина, 2iP, хлорида 2-метоксиэтилртути, 2-фенилфенола, 3,4-DA, 3,4-DB, 3,4-DP, 4-аминопиридина, 4-CPA, 4-CPA-калия, 4-CPA-натрия, 4-CPB, 4-CPP, 4-гидроксифенэтилового спирта, 8-гидроксихинолинсульфата, 8-фенилмеркуриоксихинолина, абамектина, абсцизиновой кислоты, ACC, ацефата, ацехиноцила, ацетамиприда, ацетиона, ацетохлора, ацетофоса, ацетопрола, ацибензолара, ацибензолар-S-метила, ацифлуорфена, ацифлуорфен-метила, ацифлуорфен-натрия, аклонифена, акрепа, акринатрина, акролеина, акрилонитрила, аципетакса, аципетакс-меди, аципетакс-цинка, алахлора, аланикарба, альбендазола, альдикарба, альдиморфа, альдоксикарба, альдрина, аллетрина, аллицина, аллидохлора, аллосамидина, аллоксидима, аллоксидим-натрия, аллилового спирта, алликсикарба, алорака, альфа-циперметрина, альфа-эндосульфана, аметокрадина, аметридиона, аметрина, амибузина, амикарбазона, амикартиазола, амидитиона, амидофлумета, амидосульфурона, аминокарба, аминоциклопирахлора, аминоциклопирахлор-метила, аминоциклопирахлор-калия, аминопиралида, аминопиралид-калия, аминопиралид-трис(2-гидроксипропил)аммония, амипрофос-метила, амипрофоса, амисульброма, амитона, оксалата амитона, амитраза, амитрола, сульфата аммония, аммоний α-нафталинацетата, амобама, ампропилфоса, анабазина, анцимидола, анилазина, анилофоса, анизурона, антрахинона, анту, афолата, арамита, оксида мышьяка, азомата, аспирина, азулама, азулам-калия, азулам-натрия, атидатиона, атратона, атразина, ауреофунгина, авиглицина, авиглицин гидрохлорида, азаконазола, азадирахтина, азафенидина, азаметифоса, азимсульфурона, азинфос-этила, азинфос-метила, азипротрина, азитирама, азобензола, азоциклотина, азотоата, азоксистробина, бахмедеша, барбана, гексафторсиликата бария, полисульфида бария, бартрина, BCPC, бефлубутамида, беналаксила, беналаксил-M, беназолина, беназолин-диметиламмония, беназолин-этила, беназолин-калия, бенкарбазона, бенклотиаза, бендиокарба, бенфлуралина, бенфуракарба, бенфурезата, беноданила, беномила, беноксакора, беноксафоса, бенхинокса, бенсульфурона, бенсульфурон-метила, бенсулида, бенсультапа, бентуларона, бентазона, бентазон-натрия, бентиаваликарба, бентиаваликарб-изопропила, бентиазола, бентранила, бензадокс, бензадокс-аммония, бензалконий хлорида, бензамакрила, бензамакрил-изобутила, бензаморфа, бензфендизона, бензипрама, бензобициклона, бензофенапа, бензофлуора, бензогидроксамовой кислоты, бензоксимата, бензоилпропа, бензоилпроп-этила, бензтиазурона, бензилбензоата, бензиладенина, берберина, хлорида берберина, бета-цифлутрина, бета-циперметрина, бетоксазина, бициклопирона, бифеназата, бифенокса, бифентрина, бифуцзюньчжи, биланафоса, биланафос-натрия, бинапакрила, бинцинсяо, биоаллетрина, биоэтанометрина, биоперметрина, биоресметрина, бифенила, бисазира, бисмертиазола, биспирибака, биспирибак-натрия, бистрифлурона, битретанола, битионола, биксафена, бластицидин-S, боракса, бордосской смеси, борной кислоты, боскалида, брассинолида, брассинолид-этила, бревикомина, бродифакоума, брофенвалерата, брофлутрината, бромацила, бромацил-лития, бромацил-натрия, бромадиолона, брометалина, брометрина, бромфенвинфоса, бромацетамида, бромбонила, бромбутида, бромциклена, бром-DDT, бромфеноксима, бромфоса, бромфос-этила, бромпропилата, бромталонила, бромксинила, бромксинил бутирата, бромксинил гептаноата, бромксинил октаноата, бромксинил-калия, бромпиразона, бромуканозола, бронопола, букарполята, буфенкарба, буминафоса, бупиримата, бупрофезина, бургундской смеси, бусульфана, бутакарба, бутахлора, бутафенацила, бутамифоса, бутатиофоса, бутенахлора, бутетрина, бутидазола, бутиобата, бутиурона, бутокарбоксима, бутоната, бутопироноксила, бутоксикарбоксима, бутралина, бутроксидима, бутурона, бутиламина, бутилата, какодиловой кислоты, кадусафоса, кафенстроля, арсената кальция, хлората кальция, цианамида кальция, полисульфида кальция, кальвинфоса, камбендихлора, камфехлора, камфора, каптафоля, каптана, карбаморфа, карбанолята, карбарила, карбазулама, карбендазима, бензолсульфоната карбендазима, сульфита карбендазима, карбетамида, карбофупана, дисульфида углерода, тетрахлорида углерода, карбофенотиона, карбосульфана, карбоксазола, карбоксида, карбоксина, карфентразона, карфентразон-этила, карпропамида, картапа, картап-гидрохлорида, карвакрола, карвона, CDEA, целлоцидина, CEPC, цералюра, смеси Cheshunt, хинометионата, хитозана, клобентиазона, хлометоксифена, хлоразола, хлорамбетина, хлорамбетин-аммония, хлорамбетин-диоламина, хлорамбетин-метила, хлорамбетин-метиламмония, хлорамбетин-натрия, фосфорного хлорамина, хлорамфеникола, хлораниформетана, хлоранила, хлоранокрила, хлорантранилипрола, хлоразифопа, хлоразифоп-пропаргила, хлоразина, хлорбензида, хлорбензурона, хлорбициклена, хлорбромурона, хлорбуфама, хлордана, хлордекона, хлордимеформа, гидрохлорида хлордимеформа, хлоремпентрина, хлорэтоксифоса, хлоретурона, хлорфенака, хлорфенак-аммония, хлорфенак-натрия, хлорфенапира, хлорфеназола, хлорфенетола, хлорфенпропа, хлорфенсона, хлорфенсульфида, хлорфенвинфоса, хлорфлуазурона, хлорфлуразола, хлорфлурена, хлорфлурен-метила, хлорфлуренола, хлорфлуренол-метила, хлоридазона, хлоримурона, хлоримурон-этила, хлормефоса, хлормекван, хлормекван хлорида, хлорнидина, хлорнитрофена, хлорбензилата, хлординитронафталенов, хлороформа, хлормебуформа, хлорметиурона, хлорнеба, хлорфацинона, хлорфацинон-натрия, хлорпикрина, хлоропона, хлорпропилята, хлорталонила, хлортолурона, хлороксурона, хлороксинила, хлорфония, хлорфоний хлорида, хлорфоксима, хлорпразофоса, хлорпрокарба, хлорпрофама, хлорпирифоса, хлорпирифос-метила, хлорхинокса, хлорсульфурона, хлорталя, хлорталь-диметила, хлорталь-монометила, хлортиамида, хлортиофоса, хлозолината, хлорида холина, хромафенозида, цинерина I, цинерина II, цинеринов, цинидон-этила, цинметилина, циносульфурона, циобутида, цисанилида, цисметрина, детодима, климбазола, клиодината, клодинафопа, клодинафоп-пропаргила, клоэтокарба, клофенцета, клофенцет-калия, клофентезина, клофибриновой кислоты, клофопа, клофоп-изобутила, кломазона, кломепропа, клопропа, клопоксидима, клопиралида, клопиралид-метила, клопиралидоламина, клопиралид-калия, клопиралид-трис(2-гидроксипропил)аммония, клохинтоцета, клохинтоцет-мексила, клорансулама, клорансулам-метила, клозантела, клотианидина, клотримазола, клоксифонака, клоксифонак-натрия, CMA, кодлелура, колофоната, ацетата меди, ацетоарсенита меди, арсената меди, карбоната меди, основания, гидроксида меди, нафталената меди, олеата меди, оксихлорида меди, силиката меди, сульфата меди, хромата цинка и меди, кумахлора, кумафурала, кумафоса, куматетралила, кумитоата, кумоксистробина, CPMC, CPMF, CPPC, кредазина, крезола, кримидина, кротамина, кротоксифоса, круфомата, криолита, цуэ-луре, куфранеба, кумулурона, купробама, меднистого оксида, куркуменола, цианамида, цианатрина, цианазина, цианофенфоса, цианофоса, циантоата, циантранилипрола, циазофамида, цибутрина, циклафурамида, цикланилида, циклетрина, циклоата, циклогексимида, циклопрата, циклопротрина, циклосульфамурона, циклоксаприда, циклоксидима, циклурона, циенопирафена, цифлуфенамида, цифлуметофена, цифлутрина, цигалофопа, цигалофоп-бутила, цигалотрина, цигексатин, цимиазола, цимиазол гидрохлорида, цимоксанила, циометринила, ципендазола, циперметрина, циперкват, циперкват хлорида, цифенотрина, ципразина, ципразола, ципроконазола, ципродинила, ципрофурама, ципромида, ципросульфамида, циромазина, цитиоата, диамурона, далапона, далапон-кальция, далапон-магния, далапон-натрия, даминозида, даютуна, дазомета, дазомет-натрия, DBCP, d-камфора, DCIP, DCPTA, DDT, дебакарба, декафентина, декарбофурана, дегидроуксусной кислоты, делахлора, дельтаметрина, демефиона, демефион-O, демефион-S, деметона, деметон-метила, деметон-O, деметон-O-метила, деметон-S, деметон-S-метила, деметон-S-метилсульфона, десмедифама, десметрина, d-фаньшилуцюэбинцзюйчжи, диафентиурона, диалифоса, ди-аллата, диамидафоса, диатомитовой земли, диазинона, дибутилфталата, дибутилсукцината, дикамба, дикамба-дигликольамина, дикамба-диметиламмония, дикамба-диоламина, дикамба-изопропиламмония, дикамба-метила, дикамба-оламина, дикамба-калия, дикамба-натрия, дикамба-троламина, дикаптона, дихлобенила, дихлофентиона, дихлофлуанида, дихлона, дихлоральмочевины, дихлорбензурона, дихлорфлуренола, дихлорфлуренол-метила, дихлормата, дихлормида, дихлорофена, дихлорпропа, дихлорпроп-2-этилгексила, дихлорпроп-бутотила, дихлорпроп-диметиламмония, дихлорпроп-этиламмония, дихлорпроп-изооктила, дихлорпроп-метила, дихлорпроп-P, дихлорпроп-P-2-этилгексила, дихлорпроп-P-диметиламмония, дихлорпроп-калия, дихлорпроп-натрия, дихлофоса, дихлозолина, диклобутразола, диклоцимета, диклофопа, диклофоп-метила, дикломезина, дикломезин-натрия, диклорана, диклосулама, дикофоля, дикумарола, дикрезила, дикротофоса, дицикланила, дициклонона, диэлдрина, диенохлора, диетамквата, диетамкват дихлорида, диэтатила, диэтатил-этила, диетофенкарба, диетолята, диэтилпирокарбоната, диэтилтолуамида, дифенакума, дифеноконазола, дифенопентена, дифенопентен-этила, дифеноксурона, дифензоквата, дифензокват метилсульфата, дифетиалона, дифловидазина, дифлубензурона, дифлуфеникана, дифлуфензопира, дифлуфензопир-натрия, дифлуметорима, дикегулака, дикегулак-натрия, дилора, диматифа, димефлутрина, димефокса, димефурона, димепиперата, диметахлона, диметана, диметакарба, диметахлора, диметаметрина, диметенамида, диметенамид-Р, диметипина, диметиримола, диметоата, диметоморфа, диметрина, диметилкарбата, диметилфталата, диметилвинфоса, диметилана, димексано, димидазона, димоксистробина, динекса, динекс-диклексина, динцзюньэцзо, диниконазола, диниконазол-M, динитрамина, динобутона, динокапа, динокап-4, динокап-6, диноктона, динофената, динопентона, динопропа, динозама, диносеба, диносеб-ацетата, диносеб-аммония, диносеб-диоламина, диносеб-натрия, диносеб-троламина, диносульфона, динотефурана, динотерба, динотербацетата, динотербона, диофенолана, диоксабензофоса, диоксакарба, диоксатиона, дифацинона, дифацинон-натрия, дифенамида, дифенилсульфона, дифениламина, дипропалина, дипропетрина, дипиритиона, диквата, дикват дибромида, диспарлюра, дисуля, дисульфирама, дисульфотона, дисуль-натрия, диталимфоса, дитианона, дитикрофоса, дитиоэфира, дитиопира, диурона, d-лимонена, DMPA, DNOC, DNOC-аммония, DNOC-калия, DNOC-натрия, додеморфа, додеморф ацетата, додеморф бензоата, додицина, додицин гидрохлорида, додицин-натрия, додина, дофенапина, доминикалура, дорамектина, дразоксолона, DSMA, дуфулина, EBEP, EBP, экдистерона, эдифенфоса, эглиназина, эглиназин-этила, эмамектина, эмамектинбензоата, EMPC, эмпентрина, эндосульфана, эндоталя, эндоталь-диаммония, эндоталь-дикалия, эндоталь-динатрия, эндотиона, эндрина, энестробурина, EPN, эпохолиона, эпофенонана, эпоксиконазола, эприномектина, эпроназа, EPTC, эрбона, эргокальциферола, эрлуцзисяньцаоаня, эсдепаллетрина, эсфенвалерата, эспрокарба, этацелазила, этаконазола, этафоса, этема, этабоксама, этахлора, эталфлуралина, этаметсульфурона, этаметсульфурон-метила, этапрохлора, этефона, этидимурона, этиофенкарба, этиолята, этиона, этиозина, этипрола, этиримола, этоат-метила, этофумезата, этогексадиола, этопрофоса, этоксифена, этоксифен-этила, этоксихина, этоксисульфурона, этиклозата, этилформиата, этил-а-нафталинацетата, этил-DDD, этилена, этилендибромида, этилендихлорида, этиленоксида, этилицина, этилртути 2,3-дигидроксипропилмеркаптида, ацетата этилртути, бромида этилртути, хлорида этилртути, фосфата этилртути, этинофена, этнипромида, этобензанида, этофенпрокса, этоксазола, этридиазола, этримфоса, эвгенола, EXD, фамоксадона, фамфура, фенамидона, фенаминосульфа, фенамифоса, фенапанила, фенаримола, феназулама, феназафлора, феназаквина, фенбуконазола, фенбутатин оксида, фенхлоразола, фенхлоразол-этила, фенхлорфоса, фенклорима, фенетакарба, фенфлутрина, фенфурама, фенгексамида, фенитропана, фенитротиона, фэньцзюньтуна, фенобукарба, фенопропа, фенопроп-3-бутоксипропила, фенопроп-бутометила, фенопроп-бутотила, фенопроп-бутила, фенопроп-изооктила, фенопроп-метила, фенопроп-калия, фенотиокарба, феноксакрима, феноксанила, феноксапропа, феноксапроп-этила, феноксапроп-Р, феноксапроп-Р-этила, феноксасульфона, феноксикарба, фенпиклонила, фенпиритрина, фенпропатрина, фенпропидина, фенпропиморфа, фенпиразамина, фенпироксимата, фенридазона, фенридазон-калия, фенридазон-пропила, фенсона, фенсульфотиона, фентеракола, фентиапропа, фентиапроп-этила, фентиона, фентион-этила, фентина, фентинацетата, фентинхлорида, фентингидроксида, фентразамида, фентрифанила, фенурона, фенурон TCA, фенвалерата, фербама, феримзона, сульфата железа, фипронила, флампропа, флампроп-изопропила, флампроп-M, флампроп-метила, флампроп-M-изопропила, флампроп-M-метила, флазасульфурона, флокумафена, флометоквина, флоникамида, флоразулама, флуакрипирима, флуазифопа, флуазифоп-бутила, флуазифоп-метила, флуазифоп-P, флуазифоп-P-бутила, флуазинама, флуазолята, флуазурона, флубендиамида, флубензимина, флукарбазона, флукарбазон-натрия, флуцетосульфурона, флухлоралина, флукофурона, флуциклоксурона, флуцитрината, флудиоксонила, флуенетила, флуенсульфона, флуфенацета, флуфенерима, флуфеникана, флуфеноксурона, флуфенпрокса, флуфенпира, флуфенпир-этила, флуфипрола, флуметрина, флуметовера, флуметралина, флуметсулама, флумезина, флумикролака, флумикролак-пентила, флумоксазина, флумипропина, флуморфа, флуометурона, флуопиколида, флуопирама, флуорбензида, флуоридамида, фторацетамида, флуордифена, флуоргликофена, флуоргликофен-этила, фторимида, фтормидина, фторнитрофена, флуотриурона, флуотримазола, флуоксастробина, флупоксама, флупропацила, флупропадина, флупропаната, флупропанат-натрия, флупирадифурона, флупирсульфурона, флупирсульфурон-метила, флупирсульфурон-метил-натрия, флухинконазола, флуразола, флуренола, флуренол-бутила, флуренол-метила, флуридона, флурохлоридона, флуроксипира, флуроксипир-бутометила, флуроксипир-мептила, флурпримидола, флурсуламида, флуртамона, флусиазона, флусульфамида, флутиацета, флутиацет-метила, флутианила, флутоланила, флутриафола, флувалината, флуксапироксалида, флуксофенима, фолпета, фомезафена, фомезафен-натрия, фонофоса, форамсульфурона, форхлорфенурона, формальдегида, форметаната, форметанат гидрохлорида, формотиона, формпараната, формпаранат гидрохлорида, фозамина, фозамин-аммония, фозетила, фозетил-алюминия, фозметилана, фоспирата, фостиазата, фостиэтана, фронталина, фуберидазола, фуцаоцзина, фуцаоми, фунайхэцаолина, фуфентиомочевины, фуралана, фуралаксила, фураметрина, фураметпира, фуратиокарба, фуракарбанила, фурконазола, фурконазол-цис, фуфетрина, фурфураля, фурилазола, фурмециклоса, фурофаната, фурилоксифена, гамма-цигалотрина, гамма-HCH, генита, гибберелловой кислоты, гибереллинов, глифтора, глюфозината, глюфозинат-аммония, глюфозинат-P, глюфозинат-P-аммония, глюфозинат-Р-натрия, глиодина, глиоксима, глифосата, глифосат-диаммония, глифосат-диметиламмония, глифосат-изопропиламмония, глифосат моноаммония, глифосат-калия, глифосат-сесквинатрия, глифосат-тримезия, глифозина, госсиплюра, грандлюра, грисеофульфина, гуазатин, гуазатинацетатов, галакрината, халфенпрокса, галофенозида, галозафена, галосульфурона, галосульфурон-метила, галоксидина, галоксифопа, галоксифоп-этотила, галоксифоп-метила, галоксифоп-P, галоксифоп-P-этотила, галоксифоп-P-метила, галоксифоп-натрия, HCH, хемеля, хемпы, HEOD, гептахлора, гептенофоса, гептопаргила, гетерофоса, гексахлорацетона, гексахлорбензола, гексахлорбутадиена, гексахлорфена, гексаконазола, гексафлумурона, гексафлурата, гексалюра, гексамида, гексазинона, гексилтиофоса, гекситиазокса, HHDN, холосульфа, хуаньцайво, хуанцаолина, хуаньцзюньцзо, гидраметилнона, гидраргафена, гашеной извести, цианида водорода, гидропрена, химексазола, хинуикарба, IAA, IBA, икаридина, имазалила, имазалил нитрата, имазалил сульфата, имазаметабенза, имазаметабенз-метила, имазамокса, имазамокс-аммония, имазапика, имазапик-аммония, имазапир, имазапир-изопропиламмония, имазахина, имазахин-аммония, имазахин-метила, имазахин-натрия, имазетапира, имазетапир-аммония, имазосульфурона, имибенконазола, имициафоса, имидаклоприда, имидаклотиза, иминоктадина, иминоктадин триацетата, иминоктадин триалбезилата, имипротрина, инабенфида, инданофана, индазифлама, индоксакарба, инезина, йодбонила, йодкарба, йодметана, йодсульфурона, йодсульфурон-метила, йодсульфурон-метил-натрия, иофенсульфурона, иофенсульфурон-натрия, иоксинила, иоксинил октаноата, иоксинил-лития, иоксинил-натрия, ипазина, ипконазола, ипфенкарбазона, ипробенофоса, ипродиона, ипроваликарба, ипримидама, ипсидиенола, ипсенола, IPSP, изамидофоса, исазофоса, изобензана, изокарбамида, изокарбофоса, изоцила, изодрина, изофенфоса, изофенфос-метила, изолана, изометиозина, изонорурона, изополината, изопрокарба, изопропалина, изопротиолана, изопротурона, изопиразама, изопиримола, изотиоата, изотианила, изоурона, изоваледиона, изоксабена, изоксахлортола, изоксадифена, изоксадифен-этила, изоксафлутола, изоксапирифопа, изоксатиона, ивермектина, изопамфоса, японилюра, япотринса, жасмолина I, жасмолина II, жасмоновой кислоты, цзяхуанчунцзуна, цзяцзицзенсяолиня, цзясяньцзюньчжи, цзецаованя, джецаоси, йодфенфоса, ювенильного гормона I, ювенильного гормона II, ювенильного гормона III, кадетрина, карбутилата, каретазана, каретазан-калия, казугамицина, казугамицин гидрохлорида, кежунлина, келевана, кетоспирадокса, кетоспирадокс-калия, кинетина, кинопрена, крезоксим-метила, куйцаоси, лактофена, лямбда цигалотрина, латилюра, арсената свинца, ленацила, лепимектина, лептофоса, линдана, линеатина, линурона, лиримфоса, литлура, луплура, луфенурона, лвдинцзюньчжи, лвсяньцаолина, литидатиона, МАА, малатиона, гидразида малеиновой кислоты, малонобена, мальтодекстрина, MAMA, манкупера, манкозеба, мандипропамида, манеба, матрина, мазидокса, MCPA, MCPA-2-этилгексила, MCPA-бутотила, MCPA-бутила, MCPA-диметиламмония, MCPA-диоламина, MCPA-этила, MCPA-изобутила, MCPA-изооктила, MCPA-изопропила, MCPA-метила, MCPA-оламина, MCPA-калия, MCPA-натрия, MCPA-тиоэтила, MCPA-троламина, MCPB, MCPB-этила, MCPB-метила, MCPB-натрия, мебенила, мекарбама, мекарбинзида, мекарфона, мекопропа, мекопроп-2-этилгексила, мекопроп-диметиламмония, мекопроп-диоламина, мекопроп-этадила, мекопроп-изооктила, мекопроп-метила, мекопроп-P, мекопроп-P-2-этилгексила, мекопроп-P-диметиламмония, мекопроп-P-изобутила, мекопроп-калия, мекопроп-Р-калия, мекопроп-натрия, мекопроп-троламина, медимеформа, мединотерба, мединотерб-ацетата, медлюра, мефенацета, мефенпира, мефенпир-диэтила, мефлуидида, мефлуидид-диоламина, мефлуидид-калия, мегатомовой кислоты, меназона, мепанипирима, меперфлутрина, мефената, мефосфолана, мепиквата, мепикват хлорида, мепикват пентабората, мепронила, мептилдинокапа, дихлорида ртути, оксида ртути, хлорида ртути, мерфоса, мезопразина, мезосульфурона, мезосульфурон-метила, мезотриона, месульфена, месульфенфоса, метафлумизона, металаксил, металаксил-M, метальдегида, метама, метам-аммония, метамифопа, метамитрона, метам-калия, метам-натрия, метазахлора, метазосульфурона, метазоксолона, метконазола, метепы, метфлуразона, метабензтиазурона, метакрифоса, металпропалина, метамидофоса, метасульфокарба, метазола, метфуроксама, метидатиона, метиобенкарба, метиокарба, метиопирисульфурона, метиотепы, метиолозина, метиурона, метокротофоса, метометона, метомила, метопрена, метопротрина, метохин-бутила, метотрина, метоксихлора, метоксифенозида, метоксифенона, метилафолата, метилбромида, метилэвгенола, метилйодида, метилизотиоцианата, метилацетофоса, метилхлороформа, метилдимрона, метиленхлорида, бензоата метилртути, дициандиамида метилртути, пентахлорфеноксида метилртути, метилнеодеканамида, метирама, метобензурона, метобромурона, метофлутрина, метолахлора, метолкарба, метоминостробина, метосулама, метоксадиазона, метоксурона, метрафенона, метрибузина, метсульфовакса, метсульфурона, метсульфурон-метила, мевинфоса, мексакарбата, миешуана, милбемектина, милбемицин оксима, минеба, мипафокса, мирекса, MNAF, могучуня, молината, молосультапа, моналида, моноизурона, монохлоруксусной кислоты, монокротофоса, монолинурона, моносульфурона, моносульфурон-сложного эфира, монурона, монурона TCA, морфамквата, морфамкват дихлорида, мороксидина, мороксидин гидрохлорида, морфотиона, морзида, моксидектина, MSMA, мускалюра, миклобутанила, миклозолина, N-(этилртути)-пара-толуолсульфонанилида, набама, нафталофоса, наледа, нафталина, нафталинацетамида, нафталевого ангидрида, нафтоксиуксусных кислот, напроанилида, напроамида, напталама, напталам-натрия, натамицина, небурона, никлозамида, никлозамид-оламина, никосульфурона, никотина, нифлуридида, нипираклофена, нитенпирама, нитиазина, нитралина, нирапирина, нитрилакарба, нитрофана, нитрофлуорфена, нитростирола, нитротал-изопропила, норбормида, норфлуразона, норникотина, норурона, новалурона, новифлумурона, нуаримола, OCH, октахлордипропилового эфира, октилинона, офураса, ометоата, орбенкарба, орфралюра, орто-дихлорбензола, ортосульфамурона, орикталюра, орисастробина, оризалина, остола, острамона, оксабетринила, оксадиаргила, оксадиазона, оксадиксила, оксамата, оксамила, оксапиразона, оксапиразон-димоламина, оксапиразон-натрия, оксасульфурона, оксазикломефона, оксин-меди, оксолиновой кислоты, окспоконазола, окспоконазол фумарата, оксакарбоксина, оксидеметон-метила, оксидепрофоса, оксидисульфотона, оксифлуорфена, оксиматрина, окситетрациклина, окситетрациклин гидрохлорида, паклобутразола, пайчундина, пара-дихлорбензола, парафлурона, параквата, паракват дихлорида, паракват диметилсульфата, паратона, паратон-метила, паринола, пебулата, пефуразоата, пеларгоновой кислоты, пенконазола, пенсикурона, пендиметалина, пенфлуфена, пенфлурона, пеноксулама, пентахлорфенола, пентанохлора, пентиопирада, пентметрина, пентоксазона, перфлуидона, перметрина, петоксамида, фенамакрила, феназин оксида, фенизофама, фенкаптона, фенмедифама, фенмедифам-этила, фенобензурона, фенотрина, фенпроксида, фентоата, мочевины фенилртути, ацетата фенилртути, хлорида фенилртути, фенилртутного производного прокатехола, нитрата фенилртути, салицилата фенилртути, фората, фозацемина, фозалона, фосдифена, фосфолана, фосфолан-метила, фосглицина, фосмета, фоснихлора, фосфамидона, фосфина, фосфокарба, фосфора, фостина, фоксима, фоксим-метила, фталида, пиклорама, пиклорам-2-этилгексила, пиклорам-изооктила, пиклорам-метила, пиклорам-оламина, пиклорам-калия, пиклорам-триэтиламмония, пиклорам-трис(2-гидроксипропил)аммония, пиколинафена, пикоксистробина, пиндона, пиндон натрия, пиноксадена, пипералина, пиперонил бутоксида, пиперонил циклонена, пиперофоса, пипроктанила, пипроктанил бромида, пипротала, пириметафоса, пиримикарба, пиримиоксифоса, пиримифос-этила, пиримифос-метила, плифената, поликарбамата, полиоксинов, полиоксорима, полиоксорим-цинка, политиалана, арсенита калия, азида калия, цианата калия, гиббереллята калия, нафтената калия, полисульфида калия, тиоцианата калия, α-нафталинацетата калия, pp′-DDT, праллетрина, прекоцена I, прекоцена И, прекоцена III, претилахлора, примидофоса, пиримсульфурона, пиримсульфурон-метила, пробеназола, прохлораза, прохлораз-марганца, проклонола, проциазина, процимидона, продиамина, профенофоса, профлуазола, профлуралина, профлутрина, профоксидима, проглиназина, проглиназин-этила, прогексадиона, прогексадион-калыдия, прогидрожасмона, промацила, промекарба, прометона, прометрина, промурита, пропахлора, пропамидина, пропамидин дигидрохлорида, пропамокарба, пропамокарб гидрохлорида, пропанила, пропафоса, пропахизофопа, пропаргита, пропартрина, пропазина, пропетамфоса, профама, пропиконазола, пропинеба, пропизохлора, пропоксура, пропоксикарбазона, пропоксикарбазон-натрия, пропилизома, пропирисульфурона, пропизамида, прохиназида, просулера, просульфалина, просульфокарба, просульфурона, протидатиона, протиокарба, протиокарб гидрохлорида, протиоконазола, протиофоса, протоата, протрифенбута, проксана, проксан-натрия, принахлора, пиданона, пиметрозина, пиракарболида, пираклофоса, пираклонила, пираклостробина, пирафлуфена, пирафлуфен-этила, пирафлупрола, пирамата, пираметостробина, пираоксистробина, пирасульфотола, пиразолината, пиразофоса, пиразосульфурона, пиразосульфурон-этила, пиразотиона, пиразоксифена, пиресметрина, пиретрина I, пиретрина II, пиретринов, пирибамбенз-изопропила, пирибамбенз-пропила, пирибенкарба, пирибензоксима, пирибутикарба, пириклора, пиридабена, пиридафола, пиридалила, пиридафентиона, пиридата, пиридинитрила, пирифинокса, пирифлухиназона, пирифталида, пириметанила, пиримидифена, пирисинобака, пириминобак-метила, пиримисульфана, пиримитата, пиринурона, пириофенона, пирипрола, пирипропанола, пирипроксифена, пиритиобака, пиритиобак-натрия, пиролана, пирохилона, пироксасульфона, пирокссулама, пироксихлора, пироксифура, квассии, хинацетола, сульфата хинацетола, хиналфоса, хиналфос-метила, хиназамида, хинклорака, хинконазола, хинмерака, хинокламина, хинонамида, хинотиона, хиноксифена, хинтиофоса, хинтоцена, хизалофопа, хизалофоп-этила, хизалофоп-P, хизалофоп-P-зтил, хизалофоп-P-тефурила, цюйвэньчжи, цюйиндина, рабензазола, рафоксанида, ребемида, ресметрина, родетанила, родояпонинь-III, рибавирина, римсульфурона, ротенона, риании, сафлуфенацила, сайцзюнымао, сайсэньтуна, салициланилида, сангуинарина, сантонина, шрадана, скиллирозида, себутилазина, секбуметона, седаксана, селамектина, семиамитраза, хлорида семиамитраза, сезамекса, сезамолина, сетоксидима, шуанцзяаньцаолиня, сидурона, сиглюра, силафлуобена, силатрана, силикагеля, силтиофама, симазина, симеконазола, симетона, симетрина, синтофена, SMA, S-метолахлора, арсенита натрия, азида натрия, хлората натрия, фторида натрия, фторацетата натрия, гексафторсиликата натрия, нафтената натрия, ортофенилфеноксида натрия, пентахлорфеноксида натрия, полисульфида натрия, тиоцианата натрия, α-нафталинацетата натрия, софамида, спинеторама, спиносада, спиродиклофена, спиромезифена, спиротетрамата, спироксамина, стрептомицина, стрептомицина сесквисульфата, стрихнина, сулкатола, сулкофурона, сулкофурон-натрия, сулкотриона, фульфаллята, сульфентразона, сульфирама, сульфурамида, сульфометурона, сульфометурон-метила, сульфосульфурона, сульфотема, сульфоксафлора, сульфоксида, сульфоксима, серы, серной кислоты, сульфурилфторида, сульфгликаприна, сульфпрофоса, сультропена, свепа, тау-флувалината, таврона, тазимкарба, TCA, TCA-аммония, TCA-кальция, TCA-этадила, TCA-магния, TCA-натрия, TDE, тебуконазола, тебуфенозида, тебуфенпирада, тебуфлоквина, тебупиримфоса, тебутама, тебутиурона, теклофталама, текназена, текорама, тефлубензурона, тефлутрина, тефурилтриона, темботриона, темефоса, тепы, ТЕРР, тепралоксидима, тераллетрина, тербацила, тербукарба, тербухлора, тербуфоса, тербуметона, тербутилазина, тербутрина, тетциклациса, тетрахлорэтана, тетрахлорвинфоса, тетраконазола, тетрадифона, тетрафлурона, тетраметрина, тетраметилфлутрина, тетрамина, тетранактина, тетрасула, сульфата таллия, тенилхлора, тета-циперметрина, тиабендазола, тиаклоприда, тиадифлуора, тиаметоксама, тиапронила, тиазафлурона, тиазопира, трикрофоса, трициофена, тидиазимина, тидиазурона, тиенкарбазона, тиенкарбазон-метила, тифенсульфурона, тифенсульфурон-метила, тифлузамида, тиобенкарба, тиокарбоксима, тиохлорфенфима, тиоциклама, тиоциклам гидрохлорида, тиоциклам оксалата, тиодиазол-меди, тиодикарба, тиофанокса, тиофлуоксимата, тиогемпы, тиомерсаля, тиометона, тионазина, тиофаната, тиофанат-метила, тиохинокса, тиосемикарбазида, тиосультапа, тиосультап-диаммония, тиосультап-динатрия, тиосультап-мононатрия, тиотепы, тирама, турингинзина, тиадинила, тяоцзеаня, тиокарбазила, тиоклорима, тиоксимида, тирпата, толклофос-метила, толфенпирада, толилфлуанида, ацетата толилртути, топрамезона, тралкоксидима, тралоцитрина, тралометрина, тралопирила, трансфлутрина, трансперметрина, третамина, триаконтанола, триадимефона, триадименола, триафамона, три-аллата, триамифоса, триапентенола, триаратена, триаримола, трисульфурона, триазамата, триазбутила, триазифлама, триазофоса, триазоксида, трибенурона, трибенурон-метила, трибуфоса, оксида трибутилолова, трикамба, трихламида, трихлорофона, трихлорметафос-3, трихлорната, триклопира, триклопир-бутотила, триклопир-этила, триклопир-триэтиламмония, трициклазола, тридеморфа, тридифана, триэтазина, трифенморфа, трифенофоса, трифлоксистробина, трифлоксисульфурона, трифлоксисульфурон-натрия, трифлумизола, трифлумурона, трифлуралина, трифлусульфурона, трифлусульфурон-метила, трифопа, трифоп-метила, трифопсима, трифорина, тригидрокситриазина, тримедлюра, триметакарба, триметурона, тринексапака, тринексапак-этила, трипрена, трипропиндана, триптолида, тритака, тритиконазола, тритосульфурона, trunc-call, униконазола, униконазол-P, урбацида, уредепы, валерата, валидамицина, валифеналята, валона, вамидотиона, вангарда, ванилипрола, вернолята, винклозолина, варфарина, варфарин-калия, варфарин-натрия, сяочунлюлиня, синьцзюньаня, сивоцзюньаня, ХМС, ксилахлора, ксиленолса, ксилилкарба, ишицзина, зариламида, зеатина, цзэнсяоаня, зета-циперметрин, нафтената цинка, фосфида цинка, цинктиазола, цинеба, цирама, золапрофоса, зоксамида, цзомихуанлуна, α-хлоргидрина, α-экдизона, α-мультистриатина и α-нафталинуксусной кислоты;
III. сельскохозяйственно приемлемый носитель;
IV. биопестицид;
V. одно или несколько следующих соединений:
(a) 3-(4-хлор-2,6-диметилфенил)-4-гидрокси-8-окса-1-азаспиро[4,5]дец-3-ен-2-он;
(b) 3-(4′-хлор-2,4-диметил[1,1′-бифенил]-3-ил)-4-гидрокси-8-окса-1-азаспиро[4,5]дец-3-ен-2-он;
(c) 4-[[(6-хлор-3-пиридинил)метил]метиламино]-2(5H)-фуранон;
(d) 4-[[(6-хлор-3-пиридинил)метил]циклопропиламино]-2(5H)-фуранон;
(e) 3-хлор-N2-[(1S)-1-метил-2-(метилсульфонил)этил]-N1-[2-метил-4-[1,2,2,2-тетрафтор-1-(трифторметил)этил]фенил]-1,2-бензолдикарбоксамид;
(f) 2-циано-N-этил-4-фтор-3-метоксибензолсульфонамид;
(g) 2-циано-N-этил-3-метоксибензолсульфонамид;
(h) 2-циано-3-дифторметокси-N-этил-4-фторбензолсульфонамид;
(i) 2-циано-3-фторметокси-N-этилбензолсульфонамид;
(j) 2-циано-6-фтор-3-метокси-N-диметилбензолсульфонамид;
(k) 2-циано-N-этил-6-фтор-3-метокси-N-метилбензолсульфонамид;
(l) 2-циано-3-дифторметокси-N,N-диметилбензолсульфонамид;
(m) 3-(дифторметил-N-[2-(3,3-диметилбутил)фенил]-1-метил-1Н-пиразол-4-карбоксамид;
(n) N-этил-2,2-диметилпропионамид-2-(2,6-дихлор-α,α,α-трифтор-пара-толил)гидразон;
(o) N-этил-2,2-дихлор-1-метилциклопропанкарбоксамид-2-(2,6-дихлор-α,α,α-трифтор-пара-толил)гидразонникотин;
(p) O-{(Е-)-[2-(4-хлорфенил)-2-циано-1-(2-трифторметилфенил)-винил]}S-метилтиокарбонат;
(q) (E)-N1-[(2-хлор-1,3-тиазол-5-илметил)]-N2-циано-N1-метилацетамидин;
(r) 1-(6-хлорпиридин-3-илметил)-7-метил-8-нитро-1,2,3,5,6,7-гексагидроимидазо[1,2-а]пиридин-5-ол;
(s) 4-[4-хлорфенил-(2-бутилидингидразоно)метил)]фенилмезилат; и
(t) N-этил-2,2-дихлор-1-метилциклопропанкарбоксамид-2-(2,6-дихлор-α,α,α-трифтор-пара-толил)гидразон, или
VI. семя, предпочтительно семя, которое было генетически модифицировано для выражения одного или нескольких специализированных свойств.
5. Композиция по п.1, в которой указанная молекула находится в форме пестицидно приемлемой кислотно-аддитивной соли, производного соли, гидрата,
производного сложного эфира, или кристаллического полиморфа, или
содержит 2H вместо 1H, или 14C вместо 12C.
6. Композиция по п.1, дополнительно содержащая соединение, характеризующееся одним или несколькими следующими способами действия: ингибитор ацетилхолинэстеразы; модулятор натриевого канала; ингибитор биосинтеза хитина; антагонист глутамат-зависимых хлоридных каналов и GABA; агонист глутамат-зависимых хлоридных каналов и GABA; агонист ацетилхолинового рецептора; антагонист ацетилхолинового рецептора; ингибитор MET I; ингибитор Mg-стимулированной АТФазы; никотиновый ацетилхолиновый рецептор; разрушитель клеточных мембран среднего отдела кишечника насекомых; разрушитель окислительного фосфорилирования и рианодиновый рецептор (RyRs).
7. Композиция по п.1, причем указанная композиция инкапсулирована внутри, или размещена на поверхности, капсулы, при этом указанная капсула предпочтительно характеризуется диаметром 100-900 нанометров или 10-900 мкм (микрон).
8. Способ, включающий нанесение композиции по п.1 на область для борьбы с вредителями в количестве, достаточном для борьбы с такими вредителями.
9. Способ по п.8, при котором указанный вредитель выбран из жуков, уховерток, тараканов, мух, тли, щитовок, белокрылок, цикад, муравьев, ос, термитов, моли, бабочек, вшей, кузнечиков, саранчи, сверчков, блох, трипе, щетинохвосток, клещей, зудней, нематод и сидячебрюхих, предпочтительно из типа нематоды или членистоногих, более предпочтительно из подтипа хелицеровых, мириаподов или гексаподов, даже более предпочтительно из класса арахнид, симфил или насекомых, и еще более предпочтительно из отряда вшей, отряда жесткокрылых, отряда кожистокрылых, отряда таракановых, отряда двукрылых, отряда полужесткокрылых, отряда перепончатокрылых, отряда термитов, отряда чешуекрылых, отряда пухоедов, отряда ортоптероидных, отряда блох, отряда бахромчатокрылых, отряда щетинохвосток, отряда клещей или отряда симфил, и наиболее предпочтительно представляет собой гусеницу (BAW), гусеницу совки хлопковой американской (CEW) или тлю персиковую зеленую (GPA).
10. Способ по п.8, при котором указанное количество равно от 0,01 грамма на гектар до 5000 грамм на гектар, предпочтительно от 0,1 грамма на гектар до 500 грамм на гектар, более предпочтительно от 1 грамма на гектар до 50 грамм на гектар.
11. Способ по п.8, при котором указанная область представляет собой область, на которой выращивали яблоки, кукурузу, хлопок, соевые бобы, канолу, пшеницу, рис, сорго, ячмень, овес, картофель, апельсины, люцерну, латук, клубнику, помидоры, перцы, крестоносецы, груши, табак, миндаль, сахарную свеклу или фасоль, или на которой собирались выращивать семена этого.
12. Способ по п.8, дополнительно включающий нанесение указанной композиции на генетически модифицированное растение, которое было генетически модифицировано для выражения одного или нескольких специализированных свойств.
13. Способ по п.8, при котором указанная композиция дополнительно содержит сульфат аммония.
14. Композиция по п.1 для применения для эндопаразитов, эктопаразитов, или обоих у не принадлежащего к человеческому роду животного путем перорального введения, местного нанесения или парентерального введения.
15. Способ, включающий нанесение композиции по п.1 на растение для улучшения состояния растения, выхода продукта, мощности, качества или стойкости сразу при низкой активности вредителя.
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Families Citing this family (33)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012177813A1 (en) * | 2011-06-24 | 2012-12-27 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
CA2894491A1 (en) | 2012-12-19 | 2014-06-26 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
CA2894204A1 (en) * | 2012-12-19 | 2014-08-07 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
DK2934118T5 (en) | 2012-12-19 | 2018-11-19 | Dow Agrosciences Llc | PESTICIDE COMPOSITIONS AND PROCEDURES RELATED TO IT |
US9211280B2 (en) * | 2012-12-19 | 2015-12-15 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
JP6303250B2 (ja) * | 2012-12-21 | 2018-04-04 | 石原産業株式会社 | 有害生物防除剤 |
CA2903643C (en) * | 2013-03-05 | 2022-05-24 | Bayer Cropscience Ag | Use of quinoline derivatives for improving plant yield |
CA2901474C (en) | 2013-03-14 | 2021-08-24 | Dow Agrosciences Llc | Capsule suspension formulations of dithiopyr herbicide |
CN103601714B (zh) * | 2013-08-21 | 2016-12-21 | 陕西康禾立丰生物科技药业有限公司 | 蛇床子素水剂制备方法及其组合物 |
CN103734167B (zh) * | 2014-01-10 | 2015-08-26 | 南京盈植康农业科技有限公司 | 一种含有氟啶虫胺腈的防治烟粉虱的农药制剂 |
US9078443B1 (en) | 2014-01-31 | 2015-07-14 | Fmc Corporation | Methods for controlling weeds using formulations containing fluthiacet-methyl and HPPD herbicides |
KR20170008753A (ko) * | 2014-05-16 | 2017-01-24 | 다우 아그로사이언시즈 엘엘씨 | 살충 조성물 및 관련 방법 |
TWI667224B (zh) * | 2014-06-09 | 2019-08-01 | 美商陶氏農業科學公司 | 殺蟲組成物及與其相關之方法 |
US10100526B2 (en) | 2015-05-17 | 2018-10-16 | Edward A. Knudson | Modular shelving and step assembly |
CN105052959B (zh) * | 2015-07-31 | 2017-03-01 | 山东省烟台市农业科学研究院 | 蛇床子素和噻呋酰胺的复配组合物及其应用 |
CN105123745B (zh) * | 2015-07-31 | 2017-04-19 | 广西田园生化股份有限公司 | 一种含毒氟磷和咯菌腈的杀菌组合物及杀菌剂 |
US10251394B2 (en) * | 2016-01-25 | 2019-04-09 | Dow Agrosciences Llc | Molecules having pesticidal utility, and intermediates, compositions, and processes, related thereto |
EP3407718B1 (en) * | 2016-01-25 | 2021-02-17 | Dow Agrosciences LLC | Molecules having pesticidal utility, and intermediates, compositions, and processes, related thereto |
KR20180109076A (ko) * | 2016-01-25 | 2018-10-05 | 다우 아그로사이언시즈 엘엘씨 | 살충 유용성을 갖는 분자, 및 그와 관련된 중간체, 조성물 및 방법 |
MX2018008843A (es) * | 2016-01-25 | 2019-03-06 | Dow Agrosciences Llc | Moléculas que tienen utilidad plaguicida, e intermediarios, composiciones y procesos, relacionados con ellas. |
KR102652142B1 (ko) * | 2016-01-25 | 2024-03-29 | 코르테바 애그리사이언스 엘엘씨 | 살충 유용성을 갖는 분자, 및 그와 관련된 중간체, 조성물 및 방법 |
US10681908B2 (en) * | 2016-01-25 | 2020-06-16 | Dow Agrosciences Llc | Molecules having pesticidal utility, and intermediates, compositions, and processes, related thereto |
CN105622422B (zh) * | 2016-01-29 | 2017-12-05 | 南开大学 | 一类溴代六氢茚酮类化合物及其制备方法和用途 |
TWI780112B (zh) * | 2017-03-31 | 2022-10-11 | 美商科迪華農業科技有限責任公司 | 具有殺蟲效用之分子,及其相關之中間物、組成物暨方法 |
CN110157713A (zh) * | 2019-04-08 | 2019-08-23 | 安徽农业大学 | 玉米抗旱相关基因ZmDi19-7及其应用 |
KR102695013B1 (ko) | 2019-04-24 | 2024-08-13 | 삼성전자주식회사 | 펠리클 조립체의 제조 방법 및 포토마스크 조립체의 제조 방법 |
CN110204509B (zh) * | 2019-05-16 | 2022-05-31 | 华南农业大学 | 一种苯并噻二唑-硒纳米络合物及其制备方法和应用 |
CN113816874B (zh) * | 2021-10-30 | 2024-01-26 | 大连双硼医药化工有限公司 | 一种合成4-氰基-2-氟苄醇的工艺方法 |
EP4463000A2 (en) | 2022-01-14 | 2024-11-20 | Enko Chem, Inc. | Protoporphyrinogen oxidase inhibitors |
CN114751879B (zh) * | 2022-04-18 | 2023-06-23 | 中原工学院 | 一种呋喃基双长链季铵盐化合物、制备方法及其应用 |
WO2024134415A1 (en) * | 2022-12-20 | 2024-06-27 | Coromandel International Limited | Novel fungicidal combinations of thifluzamide |
CN116982624A (zh) * | 2023-07-29 | 2023-11-03 | 扬州大学 | 一种含脱落酸类似物amf4和吡蚜酮的杀虫组合物及其应用 |
CN117924197B (zh) * | 2024-03-21 | 2024-06-07 | 山东百农思达生物科技有限公司 | 戊唑醇的高纯度合成方法 |
Family Cites Families (35)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB8406000D0 (en) | 1984-03-07 | 1984-04-11 | Ici Plc | Olefine derivatives |
KR910000247B1 (ko) | 1985-06-20 | 1991-01-23 | 에프 엠씨 코포레이션 | 살충성 폴리할로알켄 유도체 |
GB8700838D0 (en) | 1987-01-15 | 1987-02-18 | Shell Int Research | Termiticides |
US6013836A (en) | 1992-02-28 | 2000-01-11 | Rohm And Haas Company | Insecticidal N'-substituted-N,N'-disubstitutedhydrazines |
JPH072801A (ja) * | 1993-02-28 | 1995-01-06 | Nippon Nohyaku Co Ltd | 新規トリアゾール化合物及びその製法並びに該化合物を有効成分とする抗真菌剤 |
AU692894B2 (en) * | 1994-08-04 | 1998-06-18 | Sumitomo Chemical Company, Limited | Dihalopropene compounds, insecticidal/acaricidal agents containing same, and intermediates for their production |
FR2765577A1 (fr) * | 1997-07-02 | 1999-01-08 | Hoechst Schering Agrevo Sa | Nouveaux amides aromatiques, leur procede de preparation et leur application comme pesticides |
US7375232B2 (en) * | 2001-08-15 | 2008-05-20 | E.I. Du Pont De Nemours And Company | Ortho-heterocyclic substituted aryl amides for controlling invertebrate pests |
US7683096B2 (en) * | 2001-09-18 | 2010-03-23 | Ishihara Sangyo Kaisha, Ltd. | Acid amide derivatives, process for producing these, and pest control agent containing these |
JP4300009B2 (ja) * | 2001-09-18 | 2009-07-22 | 石原産業株式会社 | 酸アミド誘導体、それらの製造方法及びそれらを含有する有害生物防除剤 |
JP2005126418A (ja) * | 2003-09-30 | 2005-05-19 | Nissan Chem Ind Ltd | 置換ベンズアニリド化合物及び有害生物防除剤 |
PL1731512T3 (pl) * | 2004-03-05 | 2015-03-31 | Nissan Chemical Ind Ltd | Związek benzamidowy podstawiony izoksazoliną i środek do kontroli szkodliwych organizmów |
ITMI20041869A1 (it) * | 2004-10-01 | 2005-01-01 | Dac Srl | Nuovi inibitori delle istone deacetilasi |
AP2007004050A0 (en) * | 2004-11-26 | 2007-06-30 | Basf Ag | Novel 2-cyano-3-(halo)alkoxy-benzenesulfonamide compounds for combating animal pests |
TWI402034B (zh) | 2005-07-28 | 2013-07-21 | Dow Agrosciences Llc | 具有被層狀液晶覆膜包覆之油球之水包油乳化劑之農用組成物 |
KR101416521B1 (ko) * | 2005-09-02 | 2014-07-16 | 닛산 가가쿠 고교 가부시키 가이샤 | 이속사졸린치환 벤즈아미드 화합물 및 유해 생물 방제제 |
JP4479917B2 (ja) * | 2005-09-02 | 2010-06-09 | 日産化学工業株式会社 | イソキサゾリン置換ベンズアミド化合物及び有害生物防除剤 |
EP1951215A4 (en) | 2005-11-03 | 2009-07-29 | Redpoint Bio Corp | HYDRAZONE DERIVATIVES AND ITS USES |
TWI430995B (zh) | 2007-06-26 | 2014-03-21 | Du Pont | 萘異唑啉無脊椎有害動物控制劑 |
US20110160054A1 (en) | 2008-08-28 | 2011-06-30 | Basf Se | Pesticidal Mixtures Comprising Cyanosulfoximine Compounds and Spinetoram |
US9278134B2 (en) | 2008-12-29 | 2016-03-08 | The Board Of Trustees Of The University Of Alabama | Dual functioning ionic liquids and salts thereof |
UA107791C2 (en) * | 2009-05-05 | 2015-02-25 | Dow Agrosciences Llc | Pesticidal compositions |
US8545652B1 (en) | 2009-12-15 | 2013-10-01 | SDCmaterials, Inc. | Impact resistant material |
JP2012017289A (ja) | 2010-07-08 | 2012-01-26 | Bayer Cropscience Ag | 殺虫性ピロリン誘導体 |
KR101802004B1 (ko) | 2010-08-31 | 2017-11-27 | 다우 아그로사이언시즈 엘엘씨 | 살충제 조성물 |
SG188620A1 (en) | 2010-09-27 | 2013-04-30 | Fujimi Inc | Surface treatment composition and surface treatment method using same |
US20120177813A1 (en) | 2010-10-17 | 2012-07-12 | Thompson Mark E | Chemical annealing method for fabrication of organic thin films for optoelectronic devices |
ES2701451T3 (es) | 2011-04-28 | 2019-02-22 | Univ Southern California | Trifluorometilaciones directas usando trifluorometano |
WO2012177813A1 (en) | 2011-06-24 | 2012-12-27 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
US9211280B2 (en) | 2012-12-19 | 2015-12-15 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
CA2894491A1 (en) | 2012-12-19 | 2014-06-26 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
DK2934118T5 (en) | 2012-12-19 | 2018-11-19 | Dow Agrosciences Llc | PESTICIDE COMPOSITIONS AND PROCEDURES RELATED TO IT |
WO2014100206A1 (en) | 2012-12-19 | 2014-06-26 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
CA2894204A1 (en) | 2012-12-19 | 2014-08-07 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
WO2014100163A1 (en) | 2012-12-19 | 2014-06-26 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
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