AR095356A1 - Mezclas plaguicidas que comprenden un compuesto de pirazol - Google Patents
Mezclas plaguicidas que comprenden un compuesto de pirazolInfo
- Publication number
- AR095356A1 AR095356A1 ARP130102191A ARP130102191A AR095356A1 AR 095356 A1 AR095356 A1 AR 095356A1 AR P130102191 A ARP130102191 A AR P130102191A AR P130102191 A ARP130102191 A AR P130102191A AR 095356 A1 AR095356 A1 AR 095356A1
- Authority
- AR
- Argentina
- Prior art keywords
- methyl
- chloro
- group
- bromo
- phenyl
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 9
- 239000000203 mixture Substances 0.000 title abstract 2
- -1 b-cyfluthrin Chemical compound 0.000 abstract 14
- 125000000217 alkyl group Chemical group 0.000 abstract 9
- HOKKPVIRMVDYPB-UVTDQMKNSA-N (Z)-thiacloprid Chemical compound C1=NC(Cl)=CC=C1CN1C(=N/C#N)/SCC1 HOKKPVIRMVDYPB-UVTDQMKNSA-N 0.000 abstract 8
- 239000005940 Thiacloprid Substances 0.000 abstract 8
- 150000003254 radicals Chemical class 0.000 abstract 7
- 125000000623 heterocyclic group Chemical group 0.000 abstract 6
- 239000005946 Cypermethrin Substances 0.000 abstract 5
- 229960005424 cypermethrin Drugs 0.000 abstract 5
- 241000193388 Bacillus thuringiensis Species 0.000 abstract 4
- 239000002253 acid Substances 0.000 abstract 4
- 229940097012 bacillus thuringiensis Drugs 0.000 abstract 4
- 125000004432 carbon atom Chemical group C* 0.000 abstract 4
- ZCVAOQKBXKSDMS-PVAVHDDUSA-N (+)-trans-(S)-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)O[C@@H]1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-PVAVHDDUSA-N 0.000 abstract 3
- NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Aalpha Natural products C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 abstract 3
- 125000001188 haloalkyl group Chemical group 0.000 abstract 3
- 229910052736 halogen Inorganic materials 0.000 abstract 3
- 150000002367 halogens Chemical class 0.000 abstract 3
- 125000005842 heteroatom Chemical group 0.000 abstract 3
- 229910052757 nitrogen Inorganic materials 0.000 abstract 3
- 229910052717 sulfur Inorganic materials 0.000 abstract 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 2
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 2
- 239000000556 agonist Substances 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 230000003281 allosteric effect Effects 0.000 abstract 2
- 229960001901 bioallethrin Drugs 0.000 abstract 2
- 230000015572 biosynthetic process Effects 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 229960001591 cyfluthrin Drugs 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 2
- 239000003112 inhibitor Substances 0.000 abstract 2
- 102000042094 ryanodine receptor (TC 1.A.3.1) family Human genes 0.000 abstract 2
- 108091052345 ryanodine receptor (TC 1.A.3.1) family Proteins 0.000 abstract 2
- ZCVAOQKBXKSDMS-AQYZNVCMSA-N (+)-trans-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-AQYZNVCMSA-N 0.000 abstract 1
- CXBMCYHAMVGWJQ-CABCVRRESA-N (1,3-dioxo-4,5,6,7-tetrahydroisoindol-2-yl)methyl (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCN1C(=O)C(CCCC2)=C2C1=O CXBMCYHAMVGWJQ-CABCVRRESA-N 0.000 abstract 1
- FJDPATXIBIBRIM-QFMSAKRMSA-N (1R)-trans-cyphenothrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 FJDPATXIBIBRIM-QFMSAKRMSA-N 0.000 abstract 1
- SBNFWQZLDJGRLK-RTWAWAEBSA-N (1R)-trans-phenothrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 SBNFWQZLDJGRLK-RTWAWAEBSA-N 0.000 abstract 1
- AGMMRUPNXPWLGF-AATRIKPKSA-N (2,3,5,6-tetrafluoro-4-methylphenyl)methyl 2,2-dimethyl-3-[(e)-prop-1-enyl]cyclopropane-1-carboxylate Chemical compound CC1(C)C(/C=C/C)C1C(=O)OCC1=C(F)C(F)=C(C)C(F)=C1F AGMMRUPNXPWLGF-AATRIKPKSA-N 0.000 abstract 1
- 125000006526 (C1-C2) alkyl group Chemical group 0.000 abstract 1
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- WCXDHFDTOYPNIE-RIYZIHGNSA-N (E)-acetamiprid Chemical compound N#C/N=C(\C)N(C)CC1=CC=C(Cl)N=C1 WCXDHFDTOYPNIE-RIYZIHGNSA-N 0.000 abstract 1
- PGOOBECODWQEAB-UHFFFAOYSA-N (E)-clothianidin Chemical compound [O-][N+](=O)\N=C(/NC)NCC1=CN=C(Cl)S1 PGOOBECODWQEAB-UHFFFAOYSA-N 0.000 abstract 1
- CFRPSFYHXJZSBI-DHZHZOJOSA-N (E)-nitenpyram Chemical compound [O-][N+](=O)/C=C(\NC)N(CC)CC1=CC=C(Cl)N=C1 CFRPSFYHXJZSBI-DHZHZOJOSA-N 0.000 abstract 1
- ZFHGXWPMULPQSE-SZGBIDFHSA-N (Z)-(1S)-cis-tefluthrin Chemical compound FC1=C(F)C(C)=C(F)C(F)=C1COC(=O)[C@@H]1C(C)(C)[C@@H]1\C=C(/Cl)C(F)(F)F ZFHGXWPMULPQSE-SZGBIDFHSA-N 0.000 abstract 1
- PCTZLSCYMRXUGW-UHFFFAOYSA-N 1,1,1,2,2-pentafluorobutane Chemical group [CH2]CC(F)(F)C(F)(F)F PCTZLSCYMRXUGW-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 1
- MEQLNUTUGWFNIB-UHFFFAOYSA-N 2-(2,2,3,3,4,4,5,5-octafluoropentyl)-2-(3,3,3-trifluoropropyl)propanedinitrile Chemical compound FC(F)C(F)(F)C(F)(F)C(F)(F)CC(C#N)(C#N)CCC(F)(F)F MEQLNUTUGWFNIB-UHFFFAOYSA-N 0.000 abstract 1
- LKKQJVYXJFYYLB-UHFFFAOYSA-N 2-amino-5-cyano-N-(1-cyclopropylethyl)-3-methylbenzamide Chemical compound C1CC1C(C)NC(=O)C1=CC(C#N)=CC(C)=C1N LKKQJVYXJFYYLB-UHFFFAOYSA-N 0.000 abstract 1
- ACUOJJBRHCFOKT-UHFFFAOYSA-N 2-amino-n-(2,2,2-trifluoroethyl)acetamide Chemical compound NCC(=O)NCC(F)(F)F ACUOJJBRHCFOKT-UHFFFAOYSA-N 0.000 abstract 1
- CJXVXIQIPJXTIC-UHFFFAOYSA-N 3-[(2-chloro-1,3-thiazol-5-yl)methyl-(2-fluoroethyl)amino]-2h-furan-5-one Chemical compound C=1C(=O)OCC=1N(CCF)CC1=CN=C(Cl)S1 CJXVXIQIPJXTIC-UHFFFAOYSA-N 0.000 abstract 1
- SNNQRPYPSAJQKV-UHFFFAOYSA-N 3-[(6-chloropyridin-3-yl)methyl-(2-fluoroethyl)amino]-2h-furan-5-one Chemical compound C=1C(=O)OCC=1N(CCF)CC1=CC=C(Cl)N=C1 SNNQRPYPSAJQKV-UHFFFAOYSA-N 0.000 abstract 1
- MUXSLIWTUSNMHK-UHFFFAOYSA-N 3-amino-3h-furan-2-one Chemical class NC1C=COC1=O MUXSLIWTUSNMHK-UHFFFAOYSA-N 0.000 abstract 1
- LDMRRGRKZRNDIN-UHFFFAOYSA-N 4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4h-1,2-oxazol-3-yl]-2-methyl-n-(2,2,2-trifluoroethyl)benzamide Chemical compound C1=C(C(=O)NCC(F)(F)F)C(C)=CC(C=2CC(ON=2)(C=2C=C(Cl)C=C(Cl)C=2)C(F)(F)F)=C1 LDMRRGRKZRNDIN-UHFFFAOYSA-N 0.000 abstract 1
- RBNPAZNNDUNPFH-UHFFFAOYSA-N 4-[5-[3-chloro-5-(trifluoromethyl)phenyl]-5-(trifluoromethyl)-4h-1,2-oxazol-3-yl]-2-methyl-n-[2-oxo-2-(2,2,2-trifluoroethylamino)ethyl]benzamide Chemical compound C1=C(C(=O)NCC(=O)NCC(F)(F)F)C(C)=CC(C=2CC(ON=2)(C=2C=C(C=C(Cl)C=2)C(F)(F)F)C(F)(F)F)=C1 RBNPAZNNDUNPFH-UHFFFAOYSA-N 0.000 abstract 1
- GCAILXOZFNNIEJ-UHFFFAOYSA-N 5-[5-(3,5-dichloro-4-fluorophenyl)-5-(trifluoromethyl)-4h-1,2-oxazol-3-yl]-2-(1,2,4-triazol-1-yl)benzonitrile Chemical compound C1=C(Cl)C(F)=C(Cl)C=C1C1(C(F)(F)F)ON=C(C=2C=C(C(=CC=2)N2N=CN=C2)C#N)C1 GCAILXOZFNNIEJ-UHFFFAOYSA-N 0.000 abstract 1
- ZOCSXAVNDGMNBV-UHFFFAOYSA-N 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)sulfinyl]-1H-pyrazole-3-carbonitrile Chemical compound NC1=C(S(=O)C(F)(F)F)C(C#N)=NN1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl ZOCSXAVNDGMNBV-UHFFFAOYSA-N 0.000 abstract 1
- FORBXGROTPOMEH-UHFFFAOYSA-N 5-bromo-2-(3-chloropyridin-2-yl)pyrazole-3-carboxylic acid Chemical compound OC(=O)C1=CC(Br)=NN1C1=NC=CC=C1Cl FORBXGROTPOMEH-UHFFFAOYSA-N 0.000 abstract 1
- IBSREHMXUMOFBB-JFUDTMANSA-N 5u8924t11h Chemical compound O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1[C@@H](OC)C[C@H](O[C@@H]2C(=C/C[C@@H]3C[C@@H](C[C@@]4(O3)C=C[C@H](C)[C@@H](C(C)C)O4)OC(=O)[C@@H]3C=C(C)[C@@H](O)[C@H]4OC\C([C@@]34O)=C/C=C/[C@@H]2C)/C)O[C@H]1C.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](O)[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 IBSREHMXUMOFBB-JFUDTMANSA-N 0.000 abstract 1
- 239000005660 Abamectin Substances 0.000 abstract 1
- 239000005875 Acetamiprid Substances 0.000 abstract 1
- 239000005652 Acrinathrin Substances 0.000 abstract 1
- 239000005874 Bifenthrin Substances 0.000 abstract 1
- FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 abstract 1
- XOLJKPPBXPIOAU-UHFFFAOYSA-N C1=CC(=C(N=C1)N2C(=CC(=N2)Br)C(=O)NC3=C(C=C(C=C3Br)Br)C(=O)N(C(=O)O)N)Cl Chemical compound C1=CC(=C(N=C1)N2C(=CC(=N2)Br)C(=O)NC3=C(C=C(C=C3Br)Br)C(=O)N(C(=O)O)N)Cl XOLJKPPBXPIOAU-UHFFFAOYSA-N 0.000 abstract 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 1
- PVRAGARAKYNTLC-UHFFFAOYSA-N CC(C1CC1)NC(C1=CC(C#N)=CC(Cl)=C1C1=C(C(N)=O)N(C2=NC=CC=C2Cl)N=C1Br)=O Chemical compound CC(C1CC1)NC(C1=CC(C#N)=CC(Cl)=C1C1=C(C(N)=O)N(C2=NC=CC=C2Cl)N=C1Br)=O PVRAGARAKYNTLC-UHFFFAOYSA-N 0.000 abstract 1
- JFLRKDZMHNBDQS-UCQUSYKYSA-N CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C(=C[C@H]3[C@@H]2CC(=O)O1)C)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C.CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C=C[C@H]3C2CC(=O)O1)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C Chemical compound CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C(=C[C@H]3[C@@H]2CC(=O)O1)C)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C.CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C=C[C@H]3C2CC(=O)O1)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C JFLRKDZMHNBDQS-UCQUSYKYSA-N 0.000 abstract 1
- 229920002101 Chitin Polymers 0.000 abstract 1
- 229940123715 Chloride channel antagonist Drugs 0.000 abstract 1
- 239000005888 Clothianidin Substances 0.000 abstract 1
- 229940126062 Compound A Drugs 0.000 abstract 1
- 239000005889 Cyantraniliprole Substances 0.000 abstract 1
- 239000005892 Deltamethrin Substances 0.000 abstract 1
- YUGWDVYLFSETPE-JLHYYAGUSA-N Empenthrin Chemical compound CC\C=C(/C)C(C#C)OC(=O)C1C(C=C(C)C)C1(C)C YUGWDVYLFSETPE-JLHYYAGUSA-N 0.000 abstract 1
- 239000005895 Esfenvalerate Substances 0.000 abstract 1
- FNELVJVBIYMIMC-UHFFFAOYSA-N Ethiprole Chemical compound N1=C(C#N)C(S(=O)CC)=C(N)N1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl FNELVJVBIYMIMC-UHFFFAOYSA-N 0.000 abstract 1
- 239000005896 Etofenprox Substances 0.000 abstract 1
- JNCMHMUGTWEVOZ-UHFFFAOYSA-N F[CH]F Chemical group F[CH]F JNCMHMUGTWEVOZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000005899 Fipronil Substances 0.000 abstract 1
- 239000005900 Flonicamid Substances 0.000 abstract 1
- 239000005901 Flubendiamide Substances 0.000 abstract 1
- 108010081348 HRT1 protein Hairy Chemical group 0.000 abstract 1
- 102100021881 Hairy/enhancer-of-split related with YRPW motif protein 1 Human genes 0.000 abstract 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 abstract 1
- 239000005906 Imidacloprid Substances 0.000 abstract 1
- 241000193386 Lysinibacillus sphaericus Species 0.000 abstract 1
- 239000005951 Methiocarb Substances 0.000 abstract 1
- 239000005918 Milbemectin Substances 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 229940123925 Nicotinic receptor agonist Drugs 0.000 abstract 1
- 229940123859 Nicotinic receptor antagonist Drugs 0.000 abstract 1
- 239000005925 Pymetrozine Substances 0.000 abstract 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 abstract 1
- VQXSOUPNOZTNAI-UHFFFAOYSA-N Pyrethrin I Natural products CC(=CC1CC1C(=O)OC2CC(=O)C(=C2C)CC=C/C=C)C VQXSOUPNOZTNAI-UHFFFAOYSA-N 0.000 abstract 1
- 239000005929 Spinetoram Substances 0.000 abstract 1
- GOENIMGKWNZVDA-OAMCMWGQSA-N Spinetoram Chemical compound CO[C@@H]1[C@H](OCC)[C@@H](OC)[C@H](C)O[C@H]1OC1C[C@H]2[C@@H]3C=C4C(=O)[C@H](C)[C@@H](O[C@@H]5O[C@H](C)[C@H](CC5)N(C)C)CCC[C@H](CC)OC(=O)CC4[C@@H]3CC[C@@H]2C1 GOENIMGKWNZVDA-OAMCMWGQSA-N 0.000 abstract 1
- 239000005930 Spinosad Substances 0.000 abstract 1
- 239000005664 Spirodiclofen Substances 0.000 abstract 1
- 239000005665 Spiromesifen Substances 0.000 abstract 1
- 239000005931 Spirotetramat Substances 0.000 abstract 1
- 240000004460 Tanacetum coccineum Species 0.000 abstract 1
- 239000005938 Teflubenzuron Substances 0.000 abstract 1
- 239000005939 Tefluthrin Substances 0.000 abstract 1
- 239000005941 Thiamethoxam Substances 0.000 abstract 1
- KVIZNNVXXNFLMU-AIIUZBJTSA-N [2,3,5,6-tetrafluoro-4-(methoxymethyl)phenyl]methyl (1r,3r)-2,2-dimethyl-3-[(e)-prop-1-enyl]cyclopropane-1-carboxylate Chemical compound FC1=C(F)C(COC)=C(F)C(F)=C1COC(=O)[C@H]1C(C)(C)[C@@H]1\C=C\C KVIZNNVXXNFLMU-AIIUZBJTSA-N 0.000 abstract 1
- MWFQAAWRPDRKDG-KOLCDFICSA-N [2,3,5,6-tetrafluoro-4-(methoxymethyl)phenyl]methyl (1r,3s)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound FC1=C(F)C(COC)=C(F)C(F)=C1COC(=O)[C@H]1C(C)(C)[C@@H]1C=C(Cl)Cl MWFQAAWRPDRKDG-KOLCDFICSA-N 0.000 abstract 1
- APEPLROGLDYWBS-UHFFFAOYSA-N [2,3,5,6-tetrafluoro-4-(methoxymethyl)phenyl]methyl 2,2,3,3-tetramethylcyclopropane-1-carboxylate Chemical compound FC1=C(F)C(COC)=C(F)C(F)=C1COC(=O)C1C(C)(C)C1(C)C APEPLROGLDYWBS-UHFFFAOYSA-N 0.000 abstract 1
- ROVGZAWFACYCSP-MQBLHHJJSA-N [2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(C\C=C/C=C)C(=O)C1 ROVGZAWFACYCSP-MQBLHHJJSA-N 0.000 abstract 1
- 229950008167 abamectin Drugs 0.000 abstract 1
- GDZNYEZGJAFIKA-UHFFFAOYSA-N acetoprole Chemical compound NC1=C(S(C)=O)C(C(=O)C)=NN1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl GDZNYEZGJAFIKA-UHFFFAOYSA-N 0.000 abstract 1
- YLFSVIMMRPNPFK-WEQBUNFVSA-N acrinathrin Chemical compound CC1(C)[C@@H](\C=C/C(=O)OC(C(F)(F)F)C(F)(F)F)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YLFSVIMMRPNPFK-WEQBUNFVSA-N 0.000 abstract 1
- 125000001118 alkylidene group Chemical group 0.000 abstract 1
- ZCVAOQKBXKSDMS-UHFFFAOYSA-N allethrin Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OC1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-UHFFFAOYSA-N 0.000 abstract 1
- 229940024113 allethrin Drugs 0.000 abstract 1
- YFXPPSKYMBTNAV-UHFFFAOYSA-N bensultap Chemical compound C=1C=CC=CC=1S(=O)(=O)SCC(N(C)C)CSS(=O)(=O)C1=CC=CC=C1 YFXPPSKYMBTNAV-UHFFFAOYSA-N 0.000 abstract 1
- OMFRMAHOUUJSGP-IRHGGOMRSA-N bifenthrin Chemical compound C1=CC=C(C=2C=CC=CC=2)C(C)=C1COC(=O)[C@@H]1[C@H](\C=C(/Cl)C(F)(F)F)C1(C)C OMFRMAHOUUJSGP-IRHGGOMRSA-N 0.000 abstract 1
- VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 abstract 1
- 229950002373 bioresmethrin Drugs 0.000 abstract 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 abstract 1
- CWFOCCVIPCEQCK-UHFFFAOYSA-N chlorfenapyr Chemical compound BrC1=C(C(F)(F)F)N(COCC)C(C=2C=CC(Cl)=CC=2)=C1C#N CWFOCCVIPCEQCK-UHFFFAOYSA-N 0.000 abstract 1
- 239000003467 chloride channel stimulating agent Substances 0.000 abstract 1
- DVBUIBGJRQBEDP-UHFFFAOYSA-N cyantraniliprole Chemical compound CNC(=O)C1=CC(C#N)=CC(C)=C1NC(=O)C1=CC(Br)=NN1C1=NC=CC=C1Cl DVBUIBGJRQBEDP-UHFFFAOYSA-N 0.000 abstract 1
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- LSFUGNKKPMBOMG-UHFFFAOYSA-N cycloprothrin Chemical compound ClC1(Cl)CC1(C=1C=CC=CC=1)C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 LSFUGNKKPMBOMG-UHFFFAOYSA-N 0.000 abstract 1
- QQODLKZGRKWIFG-QSFXBCCZSA-N cyfluthrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@@H](C#N)C1=CC=C(F)C(OC=2C=CC=CC=2)=C1 QQODLKZGRKWIFG-QSFXBCCZSA-N 0.000 abstract 1
- ZXQYGBMAQZUVMI-UNOMPAQXSA-N cyhalothrin Chemical compound CC1(C)C(\C=C(/Cl)C(F)(F)F)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 ZXQYGBMAQZUVMI-UNOMPAQXSA-N 0.000 abstract 1
- KAATUXNTWXVJKI-UHFFFAOYSA-N cypermethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-UHFFFAOYSA-N 0.000 abstract 1
- 229940008203 d-transallethrin Drugs 0.000 abstract 1
- 229960002483 decamethrin Drugs 0.000 abstract 1
- OWZREIFADZCYQD-NSHGMRRFSA-N deltamethrin Chemical compound CC1(C)[C@@H](C=C(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 OWZREIFADZCYQD-NSHGMRRFSA-N 0.000 abstract 1
- YKBZOVFACRVRJN-UHFFFAOYSA-N dinotefuran Chemical compound [O-][N+](=O)\N=C(/NC)NCC1CCOC1 YKBZOVFACRVRJN-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 1
- NYPJDWWKZLNGGM-RPWUZVMVSA-N esfenvalerate Chemical compound C=1C([C@@H](C#N)OC(=O)[C@@H](C(C)C)C=2C=CC(Cl)=CC=2)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-RPWUZVMVSA-N 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- YREQHYQNNWYQCJ-UHFFFAOYSA-N etofenprox Chemical compound C1=CC(OCC)=CC=C1C(C)(C)COCC1=CC=CC(OC=2C=CC=CC=2)=C1 YREQHYQNNWYQCJ-UHFFFAOYSA-N 0.000 abstract 1
- 229950005085 etofenprox Drugs 0.000 abstract 1
- XQUXKZZNEFRCAW-UHFFFAOYSA-N fenpropathrin Chemical compound CC1(C)C(C)(C)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 XQUXKZZNEFRCAW-UHFFFAOYSA-N 0.000 abstract 1
- 229940013764 fipronil Drugs 0.000 abstract 1
- RLQJEEJISHYWON-UHFFFAOYSA-N flonicamid Chemical compound FC(F)(F)C1=CC=NC=C1C(=O)NCC#N RLQJEEJISHYWON-UHFFFAOYSA-N 0.000 abstract 1
- ZGNITFSDLCMLGI-UHFFFAOYSA-N flubendiamide Chemical compound CC1=CC(C(F)(C(F)(F)F)C(F)(F)F)=CC=C1NC(=O)C1=CC=CC(I)=C1C(=O)NC(C)(C)CS(C)(=O)=O ZGNITFSDLCMLGI-UHFFFAOYSA-N 0.000 abstract 1
- VUWZPRWSIVNGKG-UHFFFAOYSA-N fluoromethane Chemical group F[CH2] VUWZPRWSIVNGKG-UHFFFAOYSA-N 0.000 abstract 1
- QOIYTRGFOFZNKF-UHFFFAOYSA-N flupyradifurone Chemical compound C=1C(=O)OCC=1N(CC(F)F)CC1=CC=C(Cl)N=C1 QOIYTRGFOFZNKF-UHFFFAOYSA-N 0.000 abstract 1
- 229960003692 gamma aminobutyric acid Drugs 0.000 abstract 1
- BTCSSZJGUNDROE-UHFFFAOYSA-N gamma-aminobutyric acid Chemical compound NCCCC(O)=O BTCSSZJGUNDROE-UHFFFAOYSA-N 0.000 abstract 1
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 1
- HICUREFSAIZXFQ-JOWPUVSESA-N i9z29i000j Chemical compound C1C[C@H](C)[C@@H](CC)O[C@@]21O[C@H](C\C=C(C)\[C@H](OC(=O)C(=N/OC)\C=1C=CC=CC=1)[C@@H](C)\C=C\C=C/1[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\1)O)C[C@H]4C2 HICUREFSAIZXFQ-JOWPUVSESA-N 0.000 abstract 1
- 229940056881 imidacloprid Drugs 0.000 abstract 1
- YWTYJOPNNQFBPC-UHFFFAOYSA-N imidacloprid Chemical compound [O-][N+](=O)\N=C1/NCCN1CC1=CC=C(Cl)N=C1 YWTYJOPNNQFBPC-UHFFFAOYSA-N 0.000 abstract 1
- 150000002547 isoxazolines Chemical class 0.000 abstract 1
- 150000002632 lipids Chemical class 0.000 abstract 1
- CUONGYYJJVDODC-UHFFFAOYSA-N malononitrile Chemical class N#CCC#N CUONGYYJJVDODC-UHFFFAOYSA-N 0.000 abstract 1
- YFBPRJGDJKVWAH-UHFFFAOYSA-N methiocarb Chemical compound CNC(=O)OC1=CC(C)=C(SC)C(C)=C1 YFBPRJGDJKVWAH-UHFFFAOYSA-N 0.000 abstract 1
- 150000004702 methyl esters Chemical class 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 230000000813 microbial effect Effects 0.000 abstract 1
- ZLBGSRMUSVULIE-GSMJGMFJSA-N milbemycin A3 Chemical compound O1[C@H](C)[C@@H](C)CC[C@@]11O[C@H](C\C=C(C)\C[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 ZLBGSRMUSVULIE-GSMJGMFJSA-N 0.000 abstract 1
- 125000001620 monocyclic carbocycle group Chemical group 0.000 abstract 1
- 239000000181 nicotinic agonist Substances 0.000 abstract 1
- 239000003367 nicotinic antagonist Substances 0.000 abstract 1
- 229940079888 nitenpyram Drugs 0.000 abstract 1
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- 230000010627 oxidative phosphorylation Effects 0.000 abstract 1
- 229960000490 permethrin Drugs 0.000 abstract 1
- RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000000575 pesticide Substances 0.000 abstract 1
- 229960003536 phenothrin Drugs 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 229960005235 piperonyl butoxide Drugs 0.000 abstract 1
- SMKRKQBMYOFFMU-UHFFFAOYSA-N prallethrin Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OC1C(C)=C(CC#C)C(=O)C1 SMKRKQBMYOFFMU-UHFFFAOYSA-N 0.000 abstract 1
- QHMTXANCGGJZRX-WUXMJOGZSA-N pymetrozine Chemical compound C1C(C)=NNC(=O)N1\N=C\C1=CC=CN=C1 QHMTXANCGGJZRX-WUXMJOGZSA-N 0.000 abstract 1
- HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 abstract 1
- VJFUPGQZSXIULQ-XIGJTORUSA-N pyrethrin II Chemical compound CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VJFUPGQZSXIULQ-XIGJTORUSA-N 0.000 abstract 1
- 239000002728 pyrethroid Substances 0.000 abstract 1
- 229940015367 pyrethrum Drugs 0.000 abstract 1
- 230000001105 regulatory effect Effects 0.000 abstract 1
- 229940108410 resmethrin Drugs 0.000 abstract 1
- VEMKTZHHVJILDY-FIWHBWSRSA-N resmethrin Chemical compound CC1(C)[C@H](C=C(C)C)C1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-FIWHBWSRSA-N 0.000 abstract 1
- MSHXTAQSSIEBQS-UHFFFAOYSA-N s-[3-carbamoylsulfanyl-2-(dimethylamino)propyl] carbamothioate;hydron;chloride Chemical compound [Cl-].NC(=O)SCC([NH+](C)C)CSC(N)=O MSHXTAQSSIEBQS-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- HPYNBECUCCGGPA-UHFFFAOYSA-N silafluofen Chemical compound C1=CC(OCC)=CC=C1[Si](C)(C)CCCC1=CC=C(F)C(OC=2C=CC=CC=2)=C1 HPYNBECUCCGGPA-UHFFFAOYSA-N 0.000 abstract 1
- 229940014213 spinosad Drugs 0.000 abstract 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 abstract 1
- GOLXNESZZPUPJE-UHFFFAOYSA-N spiromesifen Chemical compound CC1=CC(C)=CC(C)=C1C(C(O1)=O)=C(OC(=O)CC(C)(C)C)C11CCCC1 GOLXNESZZPUPJE-UHFFFAOYSA-N 0.000 abstract 1
- CLSVJBIHYWPGQY-GGYDESQDSA-N spirotetramat Chemical compound CCOC(=O)OC1=C(C=2C(=CC=C(C)C=2)C)C(=O)N[C@@]11CC[C@H](OC)CC1 CLSVJBIHYWPGQY-GGYDESQDSA-N 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 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 abstract 1
- 229960005199 tetramethrin Drugs 0.000 abstract 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 abstract 1
- BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 0.000 abstract 1
- QSOHVSNIQHGFJU-UHFFFAOYSA-L thiosultap disodium Chemical compound [Na+].[Na+].[O-]S(=O)(=O)SCC(N(C)C)CSS([O-])(=O)=O QSOHVSNIQHGFJU-UHFFFAOYSA-L 0.000 abstract 1
- YWSCPYYRJXKUDB-KAKFPZCNSA-N tralomethrin Chemical compound CC1(C)[C@@H](C(Br)C(Br)(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YWSCPYYRJXKUDB-KAKFPZCNSA-N 0.000 abstract 1
- DDVNRFNDOPPVQJ-HQJQHLMTSA-N transfluthrin Chemical compound CC1(C)[C@H](C=C(Cl)Cl)[C@H]1C(=O)OCC1=C(F)C(F)=CC(F)=C1F DDVNRFNDOPPVQJ-HQJQHLMTSA-N 0.000 abstract 1
Classifications
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- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/58—1,2-Diazines; Hydrogenated 1,2-diazines
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- 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
- A01N37/18—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 containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/22—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 containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides
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- A—HUMAN NECESSITIES
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- 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
- A01N37/44—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 containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
- A01N37/46—N-acyl derivatives
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- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
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- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
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- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/88—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with three ring hetero atoms
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- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
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- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/18—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, directly attached to a heterocyclic or cycloaliphatic ring
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/24—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing the groups, or; Thio analogues thereof
-
- 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
- A01N51/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds having the sequences of atoms O—N—S, X—O—S, N—N—S, O—N—N or O-halogen, regardless of the number of bonds each atom has and with no atom of these sequences forming part of a heterocyclic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- General Health & Medical Sciences (AREA)
- Zoology (AREA)
- Agronomy & Crop Science (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Reivindicación 1: Mezcla plaguicida caracterizada porque comprende como compuestos activos: 1) al menos un compuesto de pirazol A seleccionado de los compuestos de la fórmula (1) en donde R¹ es H, alquilo C₁₋₂ o alcoxi C₁₋₂-alquilo C₁₋₂; R² es CH₃, CH₂F, CHF₂ o CF₃; R³ es alquilo C₂₋₆, un radical R³ᵃ o un radical R³ᵇ; R⁴ es alquilo C₁₋₄ o un grupo mencionado para R³ᵃ; R⁵ es H, halógeno o un grupo mencionado para R⁴; R³ y R⁴, junto con el átomo de carbono al que están unidos, pueden formar un carbociclo o heterociclo monocíclico de 3 a 6 miembros, que pueden contener 1 ó 2 porciones de heteroátomos seleccionadas de N-Rᶜ, O y S(O)ₖ, en donde k es 0, 1 ó 2, y en donde el carbociclo o heterociclo es no sustituido o se puede sustituir con 1, 2, 3 ó 4 radicales Rᵃ³; R³ y R⁴, junto con el átomo de carbono al que están unidos, también pueden formar un carbociclo o heterociclo monospiro o dispiro de 5 a 10 miembros, que puede contener 1 ó 2 porciones de heteroátomos seleccionadas de N-Rᶜ, O y S(O)ᵏ, en donde k es 0, 1 ó 2, y en donde el carbociclo o heterociclo es no sustituido o se puede sustituir con 1, 2, 3 ó 4 radicales Rᵃ³; R³ᵃ se selecciona del grupo que consiste en CN, NO₂, S(O)ₙRᵇ, haloalquilo C₁₋₄, alquilo C₁₋₄ que es parcial o totalmente sustituido con Rᵃ¹, alquenilo C₂₋₆, alquinilo C₂₋₆, alcoxi C₁₆, en donde los átomos C en los tres últimos radicales mencionados pueden ser no sustituidos, o parcial o totalmente sustituidos con Rᵃ², cicloalquilo C₃₋₆ y cicloalquenilo C₅₋₆, en donde los átomos C en los dos últimos radicales mencionados pueden ser no sustituidos, o parcial o totalmente sustituidos con Rᵃ³; R³ᵇ es un carbociclo o heterociclo monospiro o dispiro de 5 a 10 miembros, que puede contener 1 ó 2 porciones de heteroátomos seleccionadas de N-Rᶜ, O y S(O)ₖ, en donde k es 0, 1 ó 2, y en donde el carbociclo o heterociclo monospiro o dispiro de 5 a 10 miembros es no sustituido o se puede sustituir con 1, 2, 3 ó 4 radicales Rᵃ³; Rᵃ¹ es CN, NO₂, C(O)NH₂, C(S)NH₂, alquil C₁₋₂carboniloxi, alcoxi C₁₋₄, haloalcoxi C₁₋₂, alquil C₁₋₂oxicarbonilo, o S(O)ₙRᵇ; Rᵃ² es halógeno o un grupo mencionado para Rᵃ¹; Rᵃ³ es halógeno, alquilo C₁₋₂, haloalquilo C₁₋₂, alcoxi C₁₋₂-alquilo C₁₋₂, alquilideno C₁₋₂, =O, =S, =NRᵇ, =NORᵇ, =NSRᵇ o un grupo mencionado para Rᵃ¹; n es 0, 1 ó 2; Rᵇ se selecciona del grupo que consiste en hidrógeno, alquilo C₁₋₂, haloalquilo C₁₋₂, cicloalquilo C₃₋₆ y alcoxi C₁₋₄; Rᶜ es hidrógeno, alquilo C₁₋₂, haloalquilo C₁₋₂, alquil C₁₋₂carbonilo y alcoxi C₁₋₂carbonilo; los estereoisómeros, las sales, los tautómeros y los N-óxidos de estos; y 2) al menos un compuesto B adicional seleccionado de los compuestos de los siguientes grupos A.1, A.2, A.3, A.4, A.5, A.6, A.7, A.8, A.9, A.10, A.11, A.12, A.13, A.14, A.15, A.16, A.17, F.1, F.2, F.3, F.4, F.5, F.6, F.7, F.8, F.9, F.10 y F.11: A.1) Compuestos de carbamato seleccionados del grupo que consiste en methiocarb y thiodicarb; A.2) Compuestos piretroides seleccionados del grupo que consiste en acrinathrin, allethrin, d-cis-trans allethrin, d-trans allethrin, bifenthrin, bioallethrin, bioallethrin S-cylclopentenyl, bioresmethrin, cycloprothrin, cyfluthrin, b-cyfluthrin, cyhalothrin, l-cyhalothrin, g-cyhalothrin, cypermethrin, a-cypermethrin, b-cypermethrin, q-cypermethrin, z-cypermethrin, cyphenothrin, deltamethrin, empenthrin, esfenvalerate, etofenprox, fenpropathrin, fenvalerate, flucythrinate, flumethrin, t-fluvalinate, halfenprox, imiprothrin, meperfluthrin, metofluthrin, permethrin, phenothrin, prallethrin, profluthrin, pyrethrin (pyrethrum), resmethrin, silafluofen, tefluthrin, tetramethylfluthrin, tetramethrin, tralomethrin y transfluthrin; A.3) Compuestos agonistas / antagonistas del receptor nicotínico seleccionados del grupo que consiste en acetamiprid, bensultap, cartap clorhidrato, clothianidin, dinotefuran, imidacloprid, thiamethoxam, nitenpyram, spinosad (agonista alostérico), spinetoram (agonista alostérico), thiacloprid, thiocyclam y thiosultap-sodium; A.4) Compuestos antagonistas del canal de cloruro regulado por GABA, seleccionados del grupo que consiste en acetoprole, ethiprole y fipronil; A.5) Activadores del canal de cloruro seleccionados del grupo que consiste en abamectin, emamectin benzoate, milbemectin y lepimectin; A.6) Desacopladores de la fosforilación oxidativa, tales como chlorfenapyr; A.7) Sinergistas, tales como butóxido de piperonilo; A.8) Bloqueadores selectivos de la alimentación, seleccionados del grupo que consiste en pymetrozine y flonicamid; A.9) Inhibidores de la síntesis de quitina, seleccionados del grupo que consiste en teflubenzuron y novaluron; A.10) Inhibidores de la biosíntesis de los lípidos, seleccionados del grupo que consiste en spirodiclofen, spiromesifen y spirotetramat; A.11) Moduladores receptores de rianodína tipo diamida - ftalamidas, seleccionadas del grupo que consiste en flubendiamide y (R)-, (S)-3-cloro-N1-{2-metil-4-[1,2,2,2-tetrafluoro-1-(trifluorometil)etil]fenil}-N2-(1-metil-2-metilsulfoniletil)ftalamida (A11.1); A.12) Compuestos de isoxazolina seleccionados del grupo que consiste en 4-[5-(3,5-diclorofenil)-5-trifluorometil-4,5-dihidro-isoxazol-3-iI]-2-metil-N-piridin-2-ilmetil-benzamida (A12.1), 4-[5-(3,5-dicloro-fenil)-5-trifluorometil-4,5-dihidro-isoxazol-3-il]-2metil-N-(2,2,2-trifluoroetil)-benzamida (A12.2), 4-[5-(3,5-dicloro-fenil)-5-trifluorometil-4,5-dihidroisoxazol-3-il]-2-metil-N-[(2,2,2-trifluoro-etilcarbamoil)-metil]-benzamida (A12.3), [(2,2,2-trifluoro-etilcarbamoil)-metil]-amida del ácido 4-[5-(3,5-dicloro-fenil)-5-trifluorometil-4,5-dihidro-isoxazol-3-il]-naftalen-1-carboxílico (A12.4); 4-[5-(3-cloro-5-trifluorometil-fenil)-5-trifluorometil-4,5-dihidro-isoxazol-3-il]-2-metil-N-[(2,2,2-trifluoro-etilcarbamoil)-metil]-benzamida (A12.5), [(2,2,2-trifluoroetilcarbamoil)-metil]-amida del ácido 4-[5-(3-cloro-5-trifluorometilfenil)-5-trifluorometil-4,5-dihidro-isoxazol-3-il]-naftalen-1-carboxílico (A12.6), 5-[5-(3,5-dicloro-4-fluorofenil)-5-trifluorometil-4,5-dihidro-isoxazol-3-il]-2-[1,2,4]triazol-1-il-benzonitrilo (A12.7) y 5-[5-(3,5-dicloro-fenil)-5-trifluorometil-4,5-dihidro-isoxazol-3-iI]-2-[1,2,4]triazol-1-il-benzonitrilo (A12.8); A.13) Moduladores receptores de rianodina tipo diamida - Compuestos de antralinamida seleccionados del grupo que consiste en chloranthraniliprole, cyantraniliprole, [4-ciano-2-(1-ciclopropiletilcarbamoil)-6-metil-fenil]-amida del ácido 5-bromo-2-(3-cloro-piridin-2-il)-2H-pirazol-3-carboxílico (A13.1), [2-cloro-4-ciano-6-(1-ciclopropil-etilcarbamoil)-fenil]-amida del ácido 5-bromo-2-(3-cloro-piridin-2-il)-2H-pirazol-3-carboxílico (A13.2), [2-bromo-4-ciano-6-(1-ciclopropil-etilcarbamoil)-fenil]-amida del ácido 5-bromo-2-(3-cloropiridin-2-il)-2H-pirazol-3-carboxílico (A13.3), [2-bromo-4-cloro-6-(1-ciclopropil-etilcarbamoil)-fenil]-amida del ácido 5-bromo-2-(3-cloro-piridin-2-il)-2H-pirazol-3-carboxílico (A13.4), [2,4-dicloro-6-(1-ciclopropil-etilcarbamoil)-fenil]-amida del ácido 5-bromo-2-(3-cloro-piridin-2-il)-2H-pirazol-3-carboxílico (A13.5), [4-cloro-2-(1-ciclopropil-etilcarbamoil)-6-metil-fenil]-amida del ácido 5-bromo-2-(3-cloro-piridin-2-il)-2H-pirazol-3-carboxílico (A13.6), metiléster del ácido N-(2-{[5-bromo-2-(3-cloro-piridin-2-il)-2H-pirazol-3-carbonil]-amino}-5-cloro-3-metil-benzoil)-hidrazincarboxílico (A13.7), metiléster del ácido N-(2-{[5-bromo-2-(3-cloro-piridin-2-il)-2H-pirazol-3-carbonil]-amino}-5-cloro-3-metil-benzoil)-N-metil-hidrazincarboxílico (A13.8), metiléster del ácido N-(2-{[5-bromo-2-(3-cloro-piridin-2-il)-2H-pirazol-3-carbonil]-amino}-5-cloro-3-metil-benzoil)N,N-dimetilhidrazincarboxílico (A13.9), metiléster del ácido N-(3,5-dibromo-2-{[5-bromo-2-(3-cloro-piridin-2-il)-2H-pirazol-3-carbonil]amino}-benzoil)-hidrazincarboxílico (A13.10), metiléster del ácido N-(3,5-dibromo-2-{[5-bromo-2-(3-cloro-piridin-2-il)-2H-pirazol-3-carbonil]-amino}-benzoil)-N-metil-hidrazincarboxílico (A13.11) y metiléster del ácido N-(3,5-dibromo-2-{[5-bromo-2-(3-cloropiridin-2-il)-2H-pirazol-3-carbonil]-amino}-benzoil)-N,N-dimetil-hidrazincarboxílico (A13.12); A.14) Compuestos de malononitrilo seleccionados del grupo que consiste en 2-(2,2,3,3,4,4,5,5-octafluoropentil)-2-(3,3,3-trifluoropropil)malononitrilo (CF₂H-CF₂-F₂-F₂-CH₂-C(CN)₂-CH₂-CH₂-CF₃) (A14.1) y 2-(2,2,3,3,4,4,5,5-octafluoropentil)-2-(3,3,4,4,4-pentafluorobutil)-malonodinitrilo (CF₂HCF₂-CF₂-CF₂-CH₂-C(CN)₂-CH₂-CH₂-CF₂-CF₃) (A14.2); A.15) Disruptores microbianos seleccionados del grupo que consiste en Bacillus thuringiensis subesp. Israelensi, Bacillus sphaericus, Bacillus thuringiensis subsp. Aizawa, Bacillus thuringiensis subesp. Kurstaki y Bacillus thuringiensis subesp. Tenebrionis; A.16) Compuestos de aminofuranona seleccionados del grupo que consiste en 4-{[(2-cloro-1,3-tiazol-5-il)metil](2-fluoroetil)amino}furan-2(5H)-ona (A16.1), 4-{[(6-cloropirid-3-il)metil](2-fluoroetil)amino}furan-2(5H)-ona (A16.2), 4-{[(6-cloropirid-3-il)metil](2,2-difluoroetil)amino}furan-2(5H)-ona (
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