HRP20041165A2 - Combinations of herbicidal aromatic carboxylic acids and safeners - Google Patents

Info

Publication number

HRP20041165A2

HRP20041165A2 HR20041165A HRP20041165A HRP20041165A2 HR P20041165 A2 HRP20041165 A2 HR P20041165A2 HR 20041165 A HR20041165 A HR 20041165A HR P20041165 A HRP20041165 A HR P20041165A HR P20041165 A2 HRP20041165 A2 HR P20041165A2

Authority

HR

Croatia

Prior art keywords

herbicide

group

alkyl

compounds

salts

Prior art date

2002-06-08

Links

• Espacenet
• Global Dossier
• Discuss

• -1 aromatic carboxylic acids Chemical class 0.000 title claims abstract description 116
• 230000002363 herbicidal effect Effects 0.000 title claims abstract description 45
• 150000001875 compounds Chemical class 0.000 claims abstract description 101
• 241000196324 Embryophyta Species 0.000 claims abstract description 59
• 150000003839 salts Chemical class 0.000 claims abstract description 38
• 244000038559 crop plants Species 0.000 claims abstract description 20
• IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 claims abstract description 19
• 238000000034 method Methods 0.000 claims abstract description 14
• 239000005504 Dicamba Substances 0.000 claims abstract description 13
• XZIDTOHMJBOSOX-UHFFFAOYSA-N 2,3,6-TBA Chemical compound OC(=O)C1=C(Cl)C=CC(Cl)=C1Cl XZIDTOHMJBOSOX-UHFFFAOYSA-N 0.000 claims abstract description 7
• HSSBORCLYSCBJR-UHFFFAOYSA-N Chloramben Chemical compound NC1=CC(Cl)=CC(C(O)=O)=C1Cl HSSBORCLYSCBJR-UHFFFAOYSA-N 0.000 claims abstract description 6
• LPHICBVNSNGWLE-UHFFFAOYSA-N 2-phenyl-1,3-dihydropyrazole-5-carboxylic acid Chemical compound N1C(C(=O)O)=CCN1C1=CC=CC=C1 LPHICBVNSNGWLE-UHFFFAOYSA-N 0.000 claims abstract description 5
• 229930192334 Auxin Natural products 0.000 claims abstract description 3
• 239000002363 auxin Substances 0.000 claims abstract description 3
• SEOVTRFCIGRIMH-UHFFFAOYSA-N indole-3-acetic acid Chemical compound C1=CC=C2C(CC(=O)O)=CNC2=C1 SEOVTRFCIGRIMH-UHFFFAOYSA-N 0.000 claims abstract description 3
• 239000000203 mixture Substances 0.000 claims description 56
• 239000004009 herbicide Substances 0.000 claims description 45
• 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 26
• 238000009472 formulation Methods 0.000 claims description 25
• 229910052736 halogen Inorganic materials 0.000 claims description 24
• 229910052739 hydrogen Inorganic materials 0.000 claims description 24
• 150000002367 halogens Chemical class 0.000 claims description 23
• 239000001257 hydrogen Substances 0.000 claims description 23
• 229910052760 oxygen Inorganic materials 0.000 claims description 18
• 125000004432 carbon atom Chemical group C* 0.000 claims description 16
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 16
• 229910052717 sulfur Inorganic materials 0.000 claims description 15
• 125000000623 heterocyclic group Chemical group 0.000 claims description 13
• 230000000694 effects Effects 0.000 claims description 11
• 229930195733 hydrocarbon Natural products 0.000 claims description 11
• 229910052757 nitrogen Inorganic materials 0.000 claims description 11
• 239000004215 Carbon black (E152) Substances 0.000 claims description 10
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 10
• 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 10
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 10
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 10
• 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 9
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 9
• 125000005842 heteroatom Chemical group 0.000 claims description 9
• 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 8
• 229910006074 SO2NH2 Inorganic materials 0.000 claims description 8
• 229910002091 carbon monoxide Inorganic materials 0.000 claims description 8
• OPGCOAPTHCZZIW-UHFFFAOYSA-N diethyl 1-(2,4-dichlorophenyl)-5-methyl-4h-pyrazole-3,5-dicarboxylate Chemical compound CCOC(=O)C1(C)CC(C(=O)OCC)=NN1C1=CC=C(Cl)C=C1Cl OPGCOAPTHCZZIW-UHFFFAOYSA-N 0.000 claims description 8
• 229920006395 saturated elastomer Polymers 0.000 claims description 8
• 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 6
• 229910052799 carbon Inorganic materials 0.000 claims description 6
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
• 125000004433 nitrogen atom Chemical group N* 0.000 claims description 6
• 125000004430 oxygen atom Chemical group O* 0.000 claims description 6
• 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 5
• 125000006648 (C1-C8) haloalkyl group Chemical group 0.000 claims description 5
• 125000006652 (C3-C12) cycloalkyl group Chemical group 0.000 claims description 5
• LFGREXWGYUGZLY-UHFFFAOYSA-N phosphoryl Chemical group [P]=O LFGREXWGYUGZLY-UHFFFAOYSA-N 0.000 claims description 5
• 230000000885 phytotoxic effect Effects 0.000 claims description 5
• 230000008569 process Effects 0.000 claims description 5
• 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 4
• 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 4
• 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 4
• JJWKPURADFRFRB-UHFFFAOYSA-N carbonyl sulfide Chemical compound O=C=S JJWKPURADFRFRB-UHFFFAOYSA-N 0.000 claims description 4
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
• 231100000208 phytotoxic Toxicity 0.000 claims description 4
• 239000000729 antidote Substances 0.000 claims description 3
• 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims description 2
• 125000004399 C1-C4 alkenyl group Chemical group 0.000 claims description 2
• 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 claims description 2
• 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 2
• 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 2
• 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 2
• OAWUUPVZMNKZRY-UHFFFAOYSA-N cyprosulfamide Chemical compound COC1=CC=CC=C1C(=O)NS(=O)(=O)C1=CC=C(C(=O)NC2CC2)C=C1 OAWUUPVZMNKZRY-UHFFFAOYSA-N 0.000 claims description 2
• 239000003974 emollient agent Substances 0.000 claims description 2
• 125000000565 sulfonamide group Chemical group 0.000 claims 3
• 150000002148 esters Chemical class 0.000 abstract description 17
• 240000007594 Oryza sativa Species 0.000 abstract description 11
• 235000007164 Oryza sativa Nutrition 0.000 abstract description 11
• 235000009566 rice Nutrition 0.000 abstract description 11
• NNYRZQHKCHEXSD-UHFFFAOYSA-N Daimuron Chemical compound C1=CC(C)=CC=C1NC(=O)NC(C)(C)C1=CC=CC=C1 NNYRZQHKCHEXSD-UHFFFAOYSA-N 0.000 abstract description 6
• BWPYBAJTDILQPY-UHFFFAOYSA-N Methoxyphenone Chemical compound C1=C(C)C(OC)=CC=C1C(=O)C1=CC=CC(C)=C1 BWPYBAJTDILQPY-UHFFFAOYSA-N 0.000 abstract description 5
• BWUPSGJXXPATLU-UHFFFAOYSA-N dimepiperate Chemical compound C=1C=CC=CC=1C(C)(C)SC(=O)N1CCCCC1 BWUPSGJXXPATLU-UHFFFAOYSA-N 0.000 abstract description 5
• GTODOEDLCNTSLG-UHFFFAOYSA-N 2h-triazole-4-carboxylic acid Chemical compound OC(=O)C1=CNN=N1 GTODOEDLCNTSLG-UHFFFAOYSA-N 0.000 abstract description 3
• LVFUUWLMDUOBLC-UHFFFAOYSA-N 4-phenyl-1h-pyrazole-5-carboxylic acid Chemical compound N1N=CC(C=2C=CC=CC=2)=C1C(=O)O LVFUUWLMDUOBLC-UHFFFAOYSA-N 0.000 abstract description 3
• VRODIKIAQUNGJI-UHFFFAOYSA-N 5-phenyl-4,5-dihydro-1,2-oxazole-3-carboxylic acid Chemical group C1C(C(=O)O)=NOC1C1=CC=CC=C1 VRODIKIAQUNGJI-UHFFFAOYSA-N 0.000 abstract description 3
• ITGSCCPVERXFGN-UHFFFAOYSA-N isoxadifen Chemical compound C1C(C(=O)O)=NOC1(C=1C=CC=CC=1)C1=CC=CC=C1 ITGSCCPVERXFGN-UHFFFAOYSA-N 0.000 abstract description 3
• VYNOULHXXDFBLU-UHFFFAOYSA-N Cumyluron Chemical compound C=1C=CC=CC=1C(C)(C)NC(=O)NCC1=CC=CC=C1Cl VYNOULHXXDFBLU-UHFFFAOYSA-N 0.000 abstract description 2
• MKQSWTQPLLCSOB-UHFFFAOYSA-N benzyl 2-chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate Chemical compound N1=C(Cl)SC(C(=O)OCC=2C=CC=CC=2)=C1C(F)(F)F MKQSWTQPLLCSOB-UHFFFAOYSA-N 0.000 abstract description 2
• 150000003254 radicals Chemical class 0.000 description 45
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
• 125000001424 substituent group Chemical group 0.000 description 11
• 238000002360 preparation method Methods 0.000 description 10
• 241000209140 Triticum Species 0.000 description 9
• 235000021307 Triticum Nutrition 0.000 description 9
• 229910052708 sodium Inorganic materials 0.000 description 9
• 239000011734 sodium Substances 0.000 description 9
• 239000000243 solution Substances 0.000 description 9
• 239000000126 substance Substances 0.000 description 9
• 239000013543 active substance Substances 0.000 description 8
• 125000000217 alkyl group Chemical group 0.000 description 8
• 239000003337 fertilizer Substances 0.000 description 8
• 240000008042 Zea mays Species 0.000 description 7
• 235000002017 Zea mays subsp mays Nutrition 0.000 description 7
• 239000008187 granular material Substances 0.000 description 7
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
• 238000002156 mixing Methods 0.000 description 7
• 239000004562 water dispersible granule Substances 0.000 description 7
• QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
• 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 6
• 239000002253 acid Substances 0.000 description 6
• 125000003342 alkenyl group Chemical group 0.000 description 6
• 125000000304 alkynyl group Chemical group 0.000 description 6
• 125000003118 aryl group Chemical group 0.000 description 6
• 235000005822 corn Nutrition 0.000 description 6
• 239000004495 emulsifiable concentrate Substances 0.000 description 6
• 239000003995 emulsifying agent Substances 0.000 description 6
• 239000002689 soil Substances 0.000 description 6
• ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 5
• 244000068988 Glycine max Species 0.000 description 5
• 235000010469 Glycine max Nutrition 0.000 description 5
• 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 description 5
• 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 5
• 235000013339 cereals Nutrition 0.000 description 5
• 239000000460 chlorine Substances 0.000 description 5
• 229910052801 chlorine Inorganic materials 0.000 description 5
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
• 238000000227 grinding Methods 0.000 description 5
• 230000012010 growth Effects 0.000 description 5
• 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 5
• 230000000116 mitigating effect Effects 0.000 description 5
• 239000000575 pesticide Substances 0.000 description 5
• 239000000843 powder Substances 0.000 description 5
• PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 4
• 240000005979 Hordeum vulgare Species 0.000 description 4
• 235000007340 Hordeum vulgare Nutrition 0.000 description 4
• 244000062793 Sorghum vulgare Species 0.000 description 4
• 125000002252 acyl group Chemical group 0.000 description 4
• 125000003545 alkoxy group Chemical group 0.000 description 4
• 150000001412 amines Chemical class 0.000 description 4
• 239000004927 clay Substances 0.000 description 4
• 125000000753 cycloalkyl group Chemical group 0.000 description 4
• JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
• WCGGWVOVFQNRRS-UHFFFAOYSA-N dichloroacetamide Chemical compound NC(=O)C(Cl)Cl WCGGWVOVFQNRRS-UHFFFAOYSA-N 0.000 description 4
• 235000014113 dietary fatty acids Nutrition 0.000 description 4
• 239000000428 dust Substances 0.000 description 4
• 239000000839 emulsion Substances 0.000 description 4
• 238000005516 engineering process Methods 0.000 description 4
• 239000000194 fatty acid Substances 0.000 description 4
• 229930195729 fatty acid Natural products 0.000 description 4
• 229910052731 fluorine Inorganic materials 0.000 description 4
• 239000011737 fluorine Substances 0.000 description 4
• 125000001072 heteroaryl group Chemical group 0.000 description 4
• 150000002431 hydrogen Chemical group 0.000 description 4
• 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 4
• 239000000463 material Substances 0.000 description 4
• 150000004702 methyl esters Chemical class 0.000 description 4
• 229920000151 polyglycol Polymers 0.000 description 4
• 239000010695 polyglycol Substances 0.000 description 4
• 239000002904 solvent Substances 0.000 description 4
• 150000003460 sulfonic acids Chemical class 0.000 description 4
• 239000004094 surface-active agent Substances 0.000 description 4
• 230000009261 transgenic effect Effects 0.000 description 4
• 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 3
• 239000005995 Aluminium silicate Substances 0.000 description 3
• OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-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
• MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
• 231100000674 Phytotoxicity Toxicity 0.000 description 3
• 239000004372 Polyvinyl alcohol Substances 0.000 description 3
• VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
• 125000001118 alkylidene group Chemical group 0.000 description 3
• 235000012211 aluminium silicate Nutrition 0.000 description 3
• 230000009286 beneficial effect Effects 0.000 description 3
• WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical class OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 3
• 125000004122 cyclic group Chemical group 0.000 description 3
• 125000000392 cycloalkenyl group Chemical group 0.000 description 3
• 239000002270 dispersing agent Substances 0.000 description 3
• 239000006185 dispersion Substances 0.000 description 3
• FOUWCSDKDDHKQP-UHFFFAOYSA-N flumioxazin Chemical compound FC1=CC=2OCC(=O)N(CC#C)C=2C=C1N(C1=O)C(=O)C2=C1CCCC2 FOUWCSDKDDHKQP-UHFFFAOYSA-N 0.000 description 3
• 238000005469 granulation Methods 0.000 description 3
• 230000003179 granulation Effects 0.000 description 3
• 125000004438 haloalkoxy group Chemical group 0.000 description 3
• 125000001188 haloalkyl group Chemical group 0.000 description 3
• 239000002917 insecticide Substances 0.000 description 3
• 239000000546 pharmaceutical excipient Substances 0.000 description 3
• 229920002451 polyvinyl alcohol Polymers 0.000 description 3
• 239000007787 solid Substances 0.000 description 3
• 238000005507 spraying Methods 0.000 description 3
• 125000005346 substituted cycloalkyl group Chemical group 0.000 description 3
• 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 description 3
• 239000000080 wetting agent Substances 0.000 description 3
• AHXUVTKVCMOKIX-UHFFFAOYSA-N 1-bromo-4-(chloromethylsulfonyl)benzene Chemical compound ClCS(=O)(=O)C1=CC=C(Br)C=C1 AHXUVTKVCMOKIX-UHFFFAOYSA-N 0.000 description 2
• 239000002794 2,4-DB Substances 0.000 description 2
• JLYFCTQDENRSOL-UHFFFAOYSA-N 2-chloro-N-(2,4-dimethylthiophen-3-yl)-N-(1-methoxypropan-2-yl)acetamide Chemical compound COCC(C)N(C(=O)CCl)C=1C(C)=CSC=1C JLYFCTQDENRSOL-UHFFFAOYSA-N 0.000 description 2
• WVQBLGZPHOPPFO-UHFFFAOYSA-N 2-chloro-N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide Chemical compound CCC1=CC=CC(C)=C1N(C(C)COC)C(=O)CCl WVQBLGZPHOPPFO-UHFFFAOYSA-N 0.000 description 2
• PVSGXWMWNRGTKE-UHFFFAOYSA-N 5-methyl-2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]pyridine-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC=C(C)C=C1C(O)=O PVSGXWMWNRGTKE-UHFFFAOYSA-N 0.000 description 2
• DVOODWOZJVJKQR-UHFFFAOYSA-N 5-tert-butyl-3-(2,4-dichloro-5-prop-2-ynoxyphenyl)-1,3,4-oxadiazol-2-one Chemical group O=C1OC(C(C)(C)C)=NN1C1=CC(OCC#C)=C(Cl)C=C1Cl DVOODWOZJVJKQR-UHFFFAOYSA-N 0.000 description 2
• WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
• VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
• FDNBWBAHQKZDSN-UHFFFAOYSA-N F5231 Chemical compound C1=C(Cl)C(NS(=O)(=O)CC)=CC(N2C(N(CCCF)N=N2)=O)=C1F FDNBWBAHQKZDSN-UHFFFAOYSA-N 0.000 description 2
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• 235000003222 Helianthus annuus Nutrition 0.000 description 2
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• LTUNNEGNEKBSEH-UHFFFAOYSA-N Prosulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)CCC(F)(F)F)=N1 LTUNNEGNEKBSEH-UHFFFAOYSA-N 0.000 description 2
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• 125000001931 aliphatic group Chemical group 0.000 description 2
• 125000003282 alkyl amino group Chemical group 0.000 description 2
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• FUHMZYWBSHTEDZ-UHFFFAOYSA-M bispyribac-sodium Chemical compound [Na+].COC1=CC(OC)=NC(OC=2C(=C(OC=3N=C(OC)C=C(OC)N=3)C=CC=2)C([O-])=O)=N1 FUHMZYWBSHTEDZ-UHFFFAOYSA-M 0.000 description 2
• 238000009835 boiling Methods 0.000 description 2
• GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
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• 150000001735 carboxylic acids Chemical class 0.000 description 2
• 239000000969 carrier Substances 0.000 description 2
• WYKYKTKDBLFHCY-UHFFFAOYSA-N chloridazon Chemical compound O=C1C(Cl)=C(N)C=NN1C1=CC=CC=C1 WYKYKTKDBLFHCY-UHFFFAOYSA-N 0.000 description 2
• JXCGFZXSOMJFOA-UHFFFAOYSA-N chlorotoluron Chemical compound CN(C)C(=O)NC1=CC=C(C)C(Cl)=C1 JXCGFZXSOMJFOA-UHFFFAOYSA-N 0.000 description 2
• 239000012141 concentrate Substances 0.000 description 2
• 125000004093 cyano group Chemical group *C#N 0.000 description 2
• 238000011161 development Methods 0.000 description 2
• 125000004663 dialkyl amino group Chemical group 0.000 description 2
• 239000003085 diluting agent Substances 0.000 description 2
• 201000010099 disease Diseases 0.000 description 2
• 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
• RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
• 150000002170 ethers Chemical class 0.000 description 2
• 125000004494 ethyl ester group Chemical group 0.000 description 2
• 241001233957 eudicotyledons Species 0.000 description 2
• 150000004665 fatty acids Chemical group 0.000 description 2
• 150000002191 fatty alcohols Chemical class 0.000 description 2
• 239000000945 filler Substances 0.000 description 2
• OQZCSNDVOWYALR-UHFFFAOYSA-N flurochloridone Chemical compound FC(F)(F)C1=CC=CC(N2C(C(Cl)C(CCl)C2)=O)=C1 OQZCSNDVOWYALR-UHFFFAOYSA-N 0.000 description 2
• 125000000524 functional group Chemical group 0.000 description 2
• 239000000417 fungicide Substances 0.000 description 2
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