UA61983C2 - Fungicidal mixture based on amide compounds and benzimidazoles or the precursors thereof - Google Patents

Fungicidal mixture based on amide compounds and benzimidazoles or the precursors thereof Download PDF

Info

Publication number: UA61983C2
Authority: UA; Ukraine
Prior art keywords: alkyl; methyl; halogen; group; benzimidazoles
Prior art date: 1997-12-18

Application number

UA2000074340A

Other languages

English (en)

Ukrainian (uk)

Original Assignee

Basf Ag

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1997-12-18

Filing date

1998-12-15

Publication date

2003-12-15

1998-12-15 Application filed by Basf Ag filed Critical Basf Ag

2003-12-15 Publication of UA61983C2 publication Critical patent/UA61983C2/uk

Links

-1 amide compounds Chemical class 0.000 title claims abstract description 80
239000000203 mixture Substances 0.000 title claims abstract description 36
230000000855 fungicidal effect Effects 0.000 title claims abstract description 10
150000001556 benzimidazoles Chemical class 0.000 title claims abstract description 8
239000002243 precursor Substances 0.000 title claims abstract 6
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 24
229910052736 halogen Inorganic materials 0.000 claims abstract description 17
150000002367 halogens Chemical class 0.000 claims abstract description 16
150000001875 compounds Chemical class 0.000 claims description 27
241000233866 Fungi Species 0.000 claims description 16
239000007787 solid Substances 0.000 claims description 6
238000000034 method Methods 0.000 claims description 5
TWFZGCMQGLPBSX-UHFFFAOYSA-N carbendazim Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 claims description 4
239000002689 soil Substances 0.000 claims description 4
HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 claims description 3
WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 claims description 3
DNBMPXLFKQCOBV-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl n-(1h-benzimidazol-2-yl)carbamate Chemical compound C1=CC=C2NC(NC(=O)OCCOCCOCC)=NC2=C1 DNBMPXLFKQCOBV-UHFFFAOYSA-N 0.000 claims description 2
239000004480 active ingredient Substances 0.000 claims description 2
UYJUZNLFJAWNEZ-UHFFFAOYSA-N fuberidazole Chemical compound C1=COC(C=2NC3=CC=CC=C3N=2)=C1 UYJUZNLFJAWNEZ-UHFFFAOYSA-N 0.000 claims description 2
239000000463 material Substances 0.000 claims description 2
239000007788 liquid Substances 0.000 claims 2
RIOXQFHNBCKOKP-UHFFFAOYSA-N benomyl Chemical compound C1=CC=C2N(C(=O)NCCCC)C(NC(=O)OC)=NC2=C1 RIOXQFHNBCKOKP-UHFFFAOYSA-N 0.000 claims 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims 1
239000004615 ingredient Substances 0.000 claims 1
238000012876 topography Methods 0.000 claims 1
125000000217 alkyl group Chemical group 0.000 abstract description 30
239000013543 active substance Substances 0.000 abstract description 27
125000001424 substituent group Chemical group 0.000 abstract description 23
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract description 15
125000003118 aryl group Chemical group 0.000 abstract description 10
125000005843 halogen group Chemical group 0.000 abstract description 9
125000003342 alkenyl group Chemical group 0.000 abstract description 7
125000003545 alkoxy group Chemical group 0.000 abstract description 7
125000000753 cycloalkyl group Chemical group 0.000 abstract description 7
125000001188 haloalkyl group Chemical group 0.000 abstract description 7
125000000304 alkynyl group Chemical group 0.000 abstract description 6
125000004435 hydrogen atom Chemical group [H]* 0.000 abstract description 6
125000004414 alkyl thio group Chemical group 0.000 abstract description 5
125000000392 cycloalkenyl group Chemical group 0.000 abstract description 5
150000003254 radicals Chemical class 0.000 abstract description 5
125000005842 heteroatom Chemical group 0.000 abstract description 4
125000001931 aliphatic group Chemical group 0.000 abstract description 3
125000004644 alkyl sulfinyl group Chemical group 0.000 abstract description 3
125000004390 alkyl sulfonyl group Chemical group 0.000 abstract description 3
125000004438 haloalkoxy group Chemical group 0.000 abstract description 3
229920006395 saturated elastomer Polymers 0.000 abstract description 3
239000000417 fungicide Substances 0.000 abstract description 2
125000004995 haloalkylthio group Chemical group 0.000 abstract description 2
229910052757 nitrogen Inorganic materials 0.000 abstract description 2
150000002391 heterocyclic compounds Chemical class 0.000 abstract 2
229910052760 oxygen Inorganic materials 0.000 abstract 2
229910052717 sulfur Inorganic materials 0.000 abstract 2
JNCMHMUGTWEVOZ-UHFFFAOYSA-N F[CH]F Chemical compound F[CH]F JNCMHMUGTWEVOZ-UHFFFAOYSA-N 0.000 abstract 1
108010081348 HRT1 protein Hairy Proteins 0.000 abstract 1
102100021881 Hairy/enhancer-of-split related with YRPW motif protein 1 Human genes 0.000 abstract 1
239000002245 particle Substances 0.000 description 27
241000196324 Embryophyta Species 0.000 description 17
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 15
239000000460 chlorine Substances 0.000 description 15
229910052801 chlorine Inorganic materials 0.000 description 15
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 15
125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 12
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 10
230000003032 phytopathogenic effect Effects 0.000 description 10
239000002253 acid Substances 0.000 description 9
150000007513 acids Chemical class 0.000 description 8
241000894007 species Species 0.000 description 8
235000013339 cereals Nutrition 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
239000006185 dispersion Substances 0.000 description 6
238000010410 dusting Methods 0.000 description 6
239000000945 filler Substances 0.000 description 6
235000013312 flour Nutrition 0.000 description 6
229910052740 iodine Inorganic materials 0.000 description 6
238000005507 spraying Methods 0.000 description 6
HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 5
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 5
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 5
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 5
229910052794 bromium Inorganic materials 0.000 description 5
239000003995 emulsifying agent Substances 0.000 description 5
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
229910052731 fluorine Inorganic materials 0.000 description 5
239000011737 fluorine Substances 0.000 description 5
238000002360 preparation method Methods 0.000 description 5
239000000047 product Substances 0.000 description 5
239000000741 silica gel Substances 0.000 description 5
229910002027 silica gel Inorganic materials 0.000 description 5
239000000243 solution Substances 0.000 description 5
235000013311 vegetables Nutrition 0.000 description 5
KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 4
239000004359 castor oil Substances 0.000 description 4
235000019438 castor oil Nutrition 0.000 description 4
125000004465 cycloalkenyloxy group Chemical group 0.000 description 4
150000002191 fatty alcohols Chemical class 0.000 description 4
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 4
125000000623 heterocyclic group Chemical group 0.000 description 4
239000001257 hydrogen Substances 0.000 description 4
229910052739 hydrogen Inorganic materials 0.000 description 4
229920005610 lignin Polymers 0.000 description 4
159000000000 sodium salts Chemical class 0.000 description 4
239000005995 Aluminium silicate Substances 0.000 description 3
235000002566 Capsicum Nutrition 0.000 description 3
241000221785 Erysiphales Species 0.000 description 3
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
240000007594 Oryza sativa Species 0.000 description 3
235000007164 Oryza sativa Nutrition 0.000 description 3
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Natural products OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 3
235000021307 Triticum Nutrition 0.000 description 3
244000098338 Triticum aestivum Species 0.000 description 3
235000012211 aluminium silicate Nutrition 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
238000002474 experimental method Methods 0.000 description 3
125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 description 3
XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 3
229920000151 polyglycol Polymers 0.000 description 3
239000010695 polyglycol Substances 0.000 description 3
125000003226 pyrazolyl group Chemical group 0.000 description 3
125000004076 pyridyl group Chemical group 0.000 description 3
235000009566 rice Nutrition 0.000 description 3
150000003839 salts Chemical group 0.000 description 3
239000002904 solvent Substances 0.000 description 3
239000000725 suspension Substances 0.000 description 3
230000002195 synergetic effect Effects 0.000 description 3
125000000335 thiazolyl group Chemical group 0.000 description 3
WHOZNOZYMBRCBL-OUKQBFOZSA-N (2E)-2-Tetradecenal Chemical compound CCCCCCCCCCC\C=C\C=O WHOZNOZYMBRCBL-OUKQBFOZSA-N 0.000 description 2
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 2
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 description 2
WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 2
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
125000006050 3-methyl-2-pentenyl group Chemical group 0.000 description 2
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
235000000832 Ayote Nutrition 0.000 description 2
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
240000008574 Capsicum frutescens Species 0.000 description 2
229920000742 Cotton Polymers 0.000 description 2
240000008067 Cucumis sativus Species 0.000 description 2
235000009849 Cucumis sativus Nutrition 0.000 description 2
240000004244 Cucurbita moschata Species 0.000 description 2
235000009854 Cucurbita moschata Nutrition 0.000 description 2
235000009804 Cucurbita pepo subsp pepo Nutrition 0.000 description 2
AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
240000005979 Hordeum vulgare Species 0.000 description 2
235000007340 Hordeum vulgare Nutrition 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
235000007688 Lycopersicon esculentum Nutrition 0.000 description 2
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
235000011430 Malus pumila Nutrition 0.000 description 2
244000070406 Malus silvestris Species 0.000 description 2
235000015103 Malus silvestris Nutrition 0.000 description 2
240000005561 Musa balbisiana Species 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
240000003768 Solanum lycopersicum Species 0.000 description 2
244000061456 Solanum tuberosum Species 0.000 description 2
235000002595 Solanum tuberosum Nutrition 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
240000006365 Vitis vinifera Species 0.000 description 2
235000014787 Vitis vinifera Nutrition 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
125000003302 alkenyloxy group Chemical group 0.000 description 2
229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 2
150000008052 alkyl sulfonates Chemical class 0.000 description 2
125000005133 alkynyloxy group Chemical group 0.000 description 2
150000001491 aromatic compounds Chemical class 0.000 description 2
MQTOSJVFKKJCRP-BICOPXKESA-N azithromycin Chemical compound O([C@@H]1[C@@H](C)C(=O)O[C@@H]([C@@]([C@H](O)[C@@H](C)N(C)C[C@H](C)C[C@@](C)(O)[C@H](O[C@H]2[C@@H]([C@H](C[C@@H](C)O2)N(C)C)O)[C@H]1C)(C)O)CC)[C@H]1C[C@@](C)(OC)[C@@H](O)[C@H](C)O1 MQTOSJVFKKJCRP-BICOPXKESA-N 0.000 description 2
235000021015 bananas Nutrition 0.000 description 2
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
239000011575 calcium Substances 0.000 description 2
159000000007 calcium salts Chemical class 0.000 description 2
OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
239000001390 capsicum minimum Substances 0.000 description 2
235000013877 carbamide Nutrition 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
125000001309 chloro group Chemical group Cl* 0.000 description 2
239000004927 clay Substances 0.000 description 2
239000007859 condensation product Chemical class 0.000 description 2
125000000000 cycloalkoxy group Chemical group 0.000 description 2
125000002933 cyclohexyloxy group Chemical group C1(CCCCC1)O* 0.000 description 2
125000001887 cyclopentyloxy group Chemical group C1(CCCC1)O* 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 2
235000013399 edible fruits Nutrition 0.000 description 2
230000000694 effects Effects 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
239000003337 fertilizer Substances 0.000 description 2
230000002538 fungal effect Effects 0.000 description 2
125000002541 furyl group Chemical group 0.000 description 2
239000008187 granular material Substances 0.000 description 2
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 2
239000011630 iodine Substances 0.000 description 2
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
229910021645 metal ion Inorganic materials 0.000 description 2
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
229920000609 methyl cellulose Polymers 0.000 description 2
239000001923 methylcellulose Substances 0.000 description 2
235000010981 methylcellulose Nutrition 0.000 description 2
239000002480 mineral oil Substances 0.000 description 2
235000010446 mineral oil Nutrition 0.000 description 2
150000007522 mineralic acids Chemical class 0.000 description 2
GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Chemical class CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 2
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 2
125000001624 naphthyl group Chemical group 0.000 description 2
125000004433 nitrogen atom Chemical group N* 0.000 description 2
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical class CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
239000003921 oil Substances 0.000 description 2
150000007524 organic acids Chemical class 0.000 description 2
235000005985 organic acids Nutrition 0.000 description 2
125000002971 oxazolyl group Chemical group 0.000 description 2
229940044654 phenolsulfonic acid Drugs 0.000 description 2
235000012015 potatoes Nutrition 0.000 description 2
239000000843 powder Substances 0.000 description 2
125000001844 prenyl group Chemical group [H]C([*])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
235000015136 pumpkin Nutrition 0.000 description 2
239000011435 rock Substances 0.000 description 2
YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
150000004760 silicates Chemical class 0.000 description 2
235000012239 silicon dioxide Nutrition 0.000 description 2
150000003460 sulfonic acids Chemical class 0.000 description 2
239000000454 talc Substances 0.000 description 2
235000012222 talc Nutrition 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
ZMZDMBWJUHKJPS-UHFFFAOYSA-N thiocyanic acid Chemical compound SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 2
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
239000008096 xylene Substances 0.000 description 2
NDVASEGYNIMXJL-UWVGGRQHSA-N (-)-sabinene Chemical compound C=C1CC[C@]2(C(C)C)[C@H]1C2 NDVASEGYNIMXJL-UWVGGRQHSA-N 0.000 description 1
WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
125000006079 1,1,2-trimethyl-2-propenyl group Chemical group 0.000 description 1
125000006059 1,1-dimethyl-2-butenyl group Chemical group 0.000 description 1
125000006033 1,1-dimethyl-2-propenyl group Chemical group 0.000 description 1
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125000006065 1,3-dimethyl-2-butenyl group Chemical group 0.000 description 1
125000006066 1,3-dimethyl-3-butenyl group Chemical group 0.000 description 1
150000000211 1-dodecanols Chemical class 0.000 description 1
FKKAGFLIPSSCHT-UHFFFAOYSA-N 1-dodecoxydodecane;sulfuric acid Chemical class OS(O)(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC FKKAGFLIPSSCHT-UHFFFAOYSA-N 0.000 description 1
125000006080 1-ethyl-1-methyl-2-propenyl group Chemical group 0.000 description 1
125000006074 1-ethyl-2-butenyl group Chemical group 0.000 description 1
125000006082 1-ethyl-2-methyl-2-propenyl group Chemical group 0.000 description 1
125000006037 1-ethyl-2-propenyl group Chemical group 0.000 description 1
125000006075 1-ethyl-3-butenyl group Chemical group 0.000 description 1
125000006218 1-ethylbutyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
125000006219 1-ethylpentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
125000006028 1-methyl-2-butenyl group Chemical group 0.000 description 1
125000006048 1-methyl-2-pentenyl group Chemical group 0.000 description 1
125000006021 1-methyl-2-propenyl group Chemical group 0.000 description 1
125000006030 1-methyl-3-butenyl group Chemical group 0.000 description 1
125000006052 1-methyl-3-pentenyl group Chemical group 0.000 description 1
125000006055 1-methyl-4-pentenyl group Chemical group 0.000 description 1
XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 1
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150000002790 naphthalenes Chemical class 0.000 description 1
125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
229910052759 nickel Inorganic materials 0.000 description 1
229910017604 nitric acid Inorganic materials 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
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239000004533 oil dispersion Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
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125000004304 oxazol-5-yl group Chemical group O1C=NC=C1* 0.000 description 1
FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
235000020232 peanut Nutrition 0.000 description 1
125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
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ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 1
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125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
125000005624 silicic acid group Chemical class 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
238000009331 sowing Methods 0.000 description 1
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235000021012 strawberries Nutrition 0.000 description 1
125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 1
125000000542 sulfonic acid group Chemical group 0.000 description 1
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
239000004308 thiabendazole Substances 0.000 description 1
235000010296 thiabendazole Nutrition 0.000 description 1
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125000001113 thiadiazolyl group Chemical group 0.000 description 1
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QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical group COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
125000001425 triazolyl group Chemical group 0.000 description 1
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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
- 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
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings

Landscapes

Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

UA2000074340A 1997-12-18 1998-12-15 Fungicidal mixture based on amide compounds and benzimidazoles or the precursors thereof UA61983C2 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE19756384		1997-12-18
PCT/EP1998/008227 WO1999031984A1 (fr)	1997-12-18	1998-12-15	Melanges fongicides a base de carboxamides de pyridine et des benzimidazoles ou leurs precurseurs

Publications (1)

Publication Number	Publication Date
UA61983C2 true UA61983C2 (en)	2003-12-15

Family

ID=7852430

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
UA2000074340A UA61983C2 (en)	1997-12-18	1998-12-15	Fungicidal mixture based on amide compounds and benzimidazoles or the precursors thereof

Country Status (26)

Country	Link
US (1)	US6569875B1 (fr)
EP (1)	EP1041884B1 (fr)
JP (1)	JP4287997B2 (fr)
KR (1)	KR100536148B1 (fr)
CN (1)	CN100353836C (fr)
AR (1)	AR014139A1 (fr)
AT (1)	ATE224642T1 (fr)
AU (1)	AU753264B2 (fr)
BR (1)	BR9813667B1 (fr)
CA (1)	CA2313187C (fr)
CZ (1)	CZ295240B6 (fr)
DE (1)	DE59805744D1 (fr)
DK (1)	DK1041884T3 (fr)
EA (1)	EA003089B1 (fr)
ES (1)	ES2184357T3 (fr)
HU (1)	HUP0004330A3 (fr)
IL (2)	IL136440A0 (fr)
NZ (1)	NZ505548A (fr)
PL (1)	PL191224B1 (fr)
PT (1)	PT1041884E (fr)
SI (1)	SI1041884T1 (fr)
SK (1)	SK284850B6 (fr)
TW (1)	TW450788B (fr)
UA (1)	UA61983C2 (fr)
WO (1)	WO1999031984A1 (fr)
ZA (1)	ZA9811558B (fr)

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CN1227235C (zh) *	1999-12-09	2005-11-16	辛根塔参与股份公司	作为杀菌剂的吡唑羧酰胺和吡唑硫代羧酰胺
JP2005511474A (ja) *	2001-01-16	2005-04-28	ビーエーエスエフアクチェンゲゼルシャフト	殺菌性混合物
AU2002229712B2 (en) *	2001-01-18	2006-12-21	Basf Aktiengesellschaft	Fungicidal mixtures from benzophenones and n-biphenyl nicotinamides
DE10250110A1 (de) *	2002-10-28	2004-05-13	Bayer Cropscience Ag	Thiazol-(bi)cycloalkyl-carboxanilide
WO2004091294A2 (fr) *	2003-04-16	2004-10-28	Basf Aktiengesellschaft	Melanges fongicides
US7338967B2 (en) *	2004-09-10	2008-03-04	Syngenta Limited	Substituted isoxazoles as fungicides
EP1813151A1 (fr) *	2006-01-26	2007-08-01	BASF Aktiengesellschaft	Mélanges fongicides à base de 1-méthylpyrazol-4-yl anilides
US20090123561A1 (en) *	2005-07-14	2009-05-14	Basf Aktiengeselllschaft	Fungicide mixtures based on 1-methyl-pyrazol-4-ylcarboxanilides
BR112018005849A2 (pt) *	2015-09-24	2018-10-09	Agriculture Victoria Serv Pty	fundos bioativos
CN106818781A (zh) *	2017-03-16	2017-06-13	安徽省农业科学院植物保护与农产品质量安全研究所	一种含噻菌灵和啶酰菌胺的杀菌组合物及其用途

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DE112337C (fr)
US4078070A (en)	1973-01-16	1978-03-07	Hoechst Aktiengesellschaft	Fungicidal dispersions
DE2301921A1 (de) *	1973-01-16	1974-07-25	Hoechst Ag	Fungizide dispersionen
DD112337A1 (fr) *	1974-07-05	1975-04-12
FI54759C (fi) *	1976-04-13	1979-03-12	Kemira Oy	Fungicid
US4118788A (en) *	1977-03-07	1978-10-03	Bell Telephone Laboratories, Incorporated	Associative information retrieval
DK140520B (da) *	1977-03-08	1979-09-24	Sadolin & Holmblad As	Fremgangsmåde til behandling af nyfældet eller nysavet træ samt middel til brug ved fremgangsmåden.
CA1112160A (fr) *	1978-05-31	1981-11-10	Michael L. Clark	Compositions fongicides
JPS56167605A (en) *	1980-05-30	1981-12-23	Nippon Nohyaku Co Ltd	Seed disinfectant
IL78825A0 (en) *	1985-06-05	1986-09-30	Uniroyal Ltd	Fungicidal compositions containing carboxamidothiazoles and a method for protecting plants utilizing same
DE256503T1 (de)	1986-08-12	1990-02-08	Mitsubishi Kasei Corp., Tokio/Tokyo	Pyridincarboxamid-derivate und ihre verwendung als fungizides mittel.
CA2081935C (fr) *	1991-11-22	2004-05-25	Karl Eicken	Derives d'anilide et leur emploi contre botrytis
TW384208B (en)	1995-09-22	2000-03-11	Basf Ag	Compositions and methods for controlling harmful fungi
DE19615977A1 (de)	1996-04-22	1997-10-23	Basf Ag	Mittel und Verfahren zur Bekämpfung von Schadpilzen

1998
- 1998-12-14 TW TW087120734A patent/TW450788B/zh active
- 1998-12-15 UA UA2000074340A patent/UA61983C2/uk unknown
- 1998-12-15 IL IL13644098A patent/IL136440A0/xx active IP Right Grant
- 1998-12-15 KR KR10-2000-7006704A patent/KR100536148B1/ko not_active IP Right Cessation
- 1998-12-15 PT PT98966622T patent/PT1041884E/pt unknown
- 1998-12-15 HU HU0004330A patent/HUP0004330A3/hu unknown
- 1998-12-15 SI SI9830181T patent/SI1041884T1/xx unknown
- 1998-12-15 CZ CZ20002250A patent/CZ295240B6/cs not_active IP Right Cessation
- 1998-12-15 ES ES98966622T patent/ES2184357T3/es not_active Expired - Lifetime
- 1998-12-15 US US09/581,431 patent/US6569875B1/en not_active Expired - Lifetime
- 1998-12-15 CN CNB988123169A patent/CN100353836C/zh not_active Expired - Lifetime
- 1998-12-15 DK DK98966622T patent/DK1041884T3/da active
- 1998-12-15 JP JP2000524997A patent/JP4287997B2/ja not_active Expired - Fee Related
- 1998-12-15 EP EP98966622A patent/EP1041884B1/fr not_active Expired - Lifetime
- 1998-12-15 WO PCT/EP1998/008227 patent/WO1999031984A1/fr active IP Right Grant
- 1998-12-15 SK SK810-2000A patent/SK284850B6/sk not_active IP Right Cessation
- 1998-12-15 NZ NZ505548A patent/NZ505548A/en unknown
- 1998-12-15 EA EA200000678A patent/EA003089B1/ru not_active IP Right Cessation
- 1998-12-15 CA CA002313187A patent/CA2313187C/fr not_active Expired - Fee Related
- 1998-12-15 DE DE59805744T patent/DE59805744D1/de not_active Expired - Lifetime
- 1998-12-15 AT AT98966622T patent/ATE224642T1/de active
- 1998-12-15 BR BRPI9813667-4A patent/BR9813667B1/pt not_active IP Right Cessation
- 1998-12-15 AU AU24138/99A patent/AU753264B2/en not_active Ceased
- 1998-12-15 PL PL341315A patent/PL191224B1/pl not_active IP Right Cessation
- 1998-12-17 ZA ZA9811558A patent/ZA9811558B/xx unknown
- 1998-12-18 AR ARP980106485A patent/AR014139A1/es active IP Right Grant
2000
- 2000-05-30 IL IL136440A patent/IL136440A/en not_active IP Right Cessation

Also Published As

Publication number	Publication date
CN1282212A (zh)	2001-01-31
TW450788B (en)	2001-08-21
CN100353836C (zh)	2007-12-12
NZ505548A (en)	2003-08-29
AU753264B2 (en)	2002-10-10
BR9813667B1 (pt)	2011-05-31
BR9813667A (pt)	2000-10-10
AR014139A1 (es)	2001-02-07
SK284850B6 (sk)	2006-01-05
KR20010033267A (ko)	2001-04-25
SK8102000A3 (en)	2000-11-07
JP2001526191A (ja)	2001-12-18
PL191224B1 (pl)	2006-03-31
EP1041884B1 (fr)	2002-09-25
ES2184357T3 (es)	2003-04-01
JP4287997B2 (ja)	2009-07-01
DE59805744D1 (de)	2002-10-31
EA200000678A1 (ru)	2000-12-25
CZ295240B6 (cs)	2005-06-15
ZA9811558B (en)	2000-06-19
WO1999031984A1 (fr)	1999-07-01
CZ20002250A3 (cs)	2001-03-14
IL136440A (en)	2006-08-01
DK1041884T3 (da)	2002-10-14
HUP0004330A2 (hu)	2001-04-28
PL341315A1 (en)	2001-04-09
CA2313187C (fr)	2008-04-22
ATE224642T1 (de)	2002-10-15
EP1041884A1 (fr)	2000-10-11
US6569875B1 (en)	2003-05-27
PT1041884E (pt)	2003-02-28
HUP0004330A3 (en)	2002-11-28
IL136440A0 (en)	2001-06-14
AU2413899A (en)	1999-07-12
KR100536148B1 (ko)	2005-12-14
CA2313187A1 (fr)	1999-07-01
EA003089B1 (ru)	2002-12-26
SI1041884T1 (en)	2002-12-31

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UA54576C2 (uk)	2003-03-17	Фунгіцидні суміші на основі амідних сполук і тетрахлорізофталонітрилу та спосіб боротьби з шкідливими грибами
UA68368C2 (en)	2004-08-16	Fungicidal mixture based on amide compounds and pyridine derivatives
UA65600C2 (uk)	2004-04-15	Фунгіцидна суміш на основі амідних сполук і похідних піридину
UA65601C2 (uk)	2004-04-15	Фунгіцидна суміш на базі амідних сполук і азолів та спосіб боротьби із шкідливими грибами
KR20060120620A (ko)	2006-11-27	아미드 화합물을 이용한 식물 생장 촉진 방법
UA65599C2 (uk)	2004-04-15	Фунгіцидна суміш на основі амідних сполук
JP2000508674A (ja)	2000-07-11	有害菌類の防除用組成物および防除方法
UA61983C2 (en)	2003-12-15	Fungicidal mixture based on amide compounds and benzimidazoles or the precursors thereof
UA55506C2 (uk)	2003-04-15	Фунгіцидна суміш на базі амідних сполук і похідних морфоліну або піперидину та спосіб боротьби з шкідливими грибами
UA61984C2 (en)	2003-12-15	Fungicide mixture based on amide compounds and (+- )-(2-chlorphenyl)(4-chlorphenyl)(pyrimidin-5-yl) methanol
EA003704B1 (ru)	2003-08-28	Фунгицидная смесь на основе амидных соединений и производных бензамидоксима
UA72237C2 (en)	2005-02-15	Fungicidal mixture and a method to control harmful fungi
MXPA00005666A (es)	2001-07-03	Mezclas fungicidas a base de compuestos de amida y tetracloroisoftalonitrilo
MXPA00005382A (en)	2001-07-03	Fungicide mixtures based on amide compounds and pyridine derivatives