KR20060131926A - 제초제-약해완화제 배합물 - Google Patents

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Publication number

KR20060131926A

KR20060131926A KR1020067020021A KR20067020021A KR20060131926A KR 20060131926 A KR20060131926 A KR 20060131926A KR 1020067020021 A KR1020067020021 A KR 1020067020021A KR 20067020021 A KR20067020021 A KR 20067020021A KR 20060131926 A KR20060131926 A KR 20060131926A

Authority

KR

South Korea

Prior art keywords

alkyl

case

halogen

hydrogen

alkoxy

Prior art date

2004-03-27

Legal status (The legal status 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 status listed.)

Ceased

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• 239000000203 mixture Substances 0.000 title claims description 39
• 238000009472 formulation Methods 0.000 title claims description 20
• 239000001257 hydrogen Substances 0.000 claims abstract description 101
• 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 101
• 150000001875 compounds Chemical class 0.000 claims abstract description 100
• 229910052736 halogen Inorganic materials 0.000 claims abstract description 79
• 150000002367 halogens Chemical class 0.000 claims abstract description 78
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 62
• 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 53
• 150000002431 hydrogen Chemical class 0.000 claims abstract description 37
• 125000003545 alkoxy group Chemical group 0.000 claims abstract description 31
• 150000003839 salts Chemical class 0.000 claims abstract description 25
• IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 24
• 125000003282 alkyl amino group Chemical group 0.000 claims abstract description 22
• 125000004414 alkyl thio group Chemical group 0.000 claims abstract description 22
• 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 21
• 125000000217 alkyl group Chemical group 0.000 claims abstract description 20
• 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 20
• 125000003342 alkenyl group Chemical group 0.000 claims abstract description 16
• 125000000304 alkynyl group Chemical group 0.000 claims abstract description 15
• 125000003118 aryl group Chemical group 0.000 claims abstract description 13
• 125000004453 alkoxycarbonyl group Chemical group 0.000 claims abstract description 12
• 125000004448 alkyl carbonyl group Chemical group 0.000 claims abstract description 12
• 125000004644 alkyl sulfinyl group Chemical group 0.000 claims abstract description 12
• 125000004390 alkyl sulfonyl group Chemical group 0.000 claims abstract description 12
• 125000004663 dialkyl amino group Chemical group 0.000 claims abstract description 12
• 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims abstract description 10
• 125000000858 thiocyanato group Chemical group *SC#N 0.000 claims abstract description 10
• 125000001188 haloalkyl group Chemical group 0.000 claims abstract description 9
• 239000002249 anxiolytic agent Substances 0.000 claims abstract description 7
• 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 7
• 125000004183 alkoxy alkyl group Chemical group 0.000 claims abstract description 5
• 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 4
• 125000002947 alkylene group Chemical group 0.000 claims abstract description 3
• 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims abstract description 3
• 239000003795 chemical substances by application Substances 0.000 claims description 34
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 29
• 238000000034 method Methods 0.000 claims description 19
• MWKVXOJATACCCH-UHFFFAOYSA-N isoxadifen-ethyl Chemical group C1C(C(=O)OCC)=NOC1(C=1C=CC=CC=1)C1=CC=CC=C1 MWKVXOJATACCCH-UHFFFAOYSA-N 0.000 claims description 17
• 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 claims description 14
• VYNOULHXXDFBLU-UHFFFAOYSA-N Cumyluron Chemical compound C=1C=CC=CC=1C(C)(C)NC(=O)NCC1=CC=CC=C1Cl VYNOULHXXDFBLU-UHFFFAOYSA-N 0.000 claims description 11
• YNQSILKYZQZHFJ-UHFFFAOYSA-N R-29148 Chemical compound CC1CN(C(=O)C(Cl)Cl)C(C)(C)O1 YNQSILKYZQZHFJ-UHFFFAOYSA-N 0.000 claims description 11
• 230000009261 transgenic effect Effects 0.000 claims description 10
• GRSMWKLPSNHDHA-UHFFFAOYSA-N Naphthalic anhydride Chemical compound C1=CC(C(=O)OC2=O)=C3C2=CC=CC3=C1 GRSMWKLPSNHDHA-UHFFFAOYSA-N 0.000 claims description 8
• XXWNKVBJDWSYBN-UHFFFAOYSA-N diethoxy-phenoxy-sulfanylidene-$l^{5}-phosphane Chemical compound CCOP(=S)(OCC)OC1=CC=CC=C1 XXWNKVBJDWSYBN-UHFFFAOYSA-N 0.000 claims description 7
• COYBRKAVBMYYSF-UHFFFAOYSA-N heptan-2-yl [(5-chloroquinolin-8-yl)oxy]acetate Chemical group C1=CN=C2C(OCC(=O)OC(C)CCCCC)=CC=C(Cl)C2=C1 COYBRKAVBMYYSF-UHFFFAOYSA-N 0.000 claims description 7
• PFJJMJDEVDLPNE-UHFFFAOYSA-N Benoxacor Chemical compound C1=CC=C2N(C(=O)C(Cl)Cl)C(C)COC2=C1 PFJJMJDEVDLPNE-UHFFFAOYSA-N 0.000 claims description 6
• UKSLKNUCVPZQCQ-UHFFFAOYSA-N Fluxofenim Chemical compound C=1C=C(Cl)C=CC=1C(C(F)(F)F)=NOCC1OCCO1 UKSLKNUCVPZQCQ-UHFFFAOYSA-N 0.000 claims description 6
• 239000000654 additive Substances 0.000 claims description 6
• OPGCOAPTHCZZIW-UHFFFAOYSA-N diethyl 1-(2,4-dichlorophenyl)-5-methyl-4h-pyrazole-3,5-dicarboxylate Chemical group CCOC(=O)C1(C)CC(C(=O)OCC)=NN1C1=CC=C(Cl)C=C1Cl OPGCOAPTHCZZIW-UHFFFAOYSA-N 0.000 claims description 6
• 235000013311 vegetables Nutrition 0.000 claims description 4
• VGQLNJWOULYVFV-WZENYGAOSA-N dimethyl (2r,3s)-bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylate Chemical compound C1C2C=CC1[C@H](C(=O)OC)[C@@H]2C(=O)OC VGQLNJWOULYVFV-WZENYGAOSA-N 0.000 claims description 3
• JCHMGYRXQDASJE-UHFFFAOYSA-N metcamifen Chemical compound C1=CC(NC(=O)NC)=CC=C1S(=O)(=O)NC(=O)C1=CC=CC=C1OC JCHMGYRXQDASJE-UHFFFAOYSA-N 0.000 claims description 3
• NYDKNJDNBUFWRJ-UHFFFAOYSA-N n-[4-(dimethylcarbamoylamino)phenyl]sulfonyl-2-methoxybenzamide Chemical compound COC1=CC=CC=C1C(=O)NS(=O)(=O)C1=CC=C(NC(=O)N(C)C)C=C1 NYDKNJDNBUFWRJ-UHFFFAOYSA-N 0.000 claims description 3
• YRMLFORXOOIJDR-UHFFFAOYSA-N Dichlormid Chemical compound ClC(Cl)C(=O)N(CC=C)CC=C YRMLFORXOOIJDR-UHFFFAOYSA-N 0.000 claims description 2
• 238000009394 selective breeding Methods 0.000 claims description 2
• -1 alkyl radical Chemical class 0.000 description 157
• 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 74
• 150000003254 radicals Chemical class 0.000 description 68
• 241000196324 Embryophyta Species 0.000 description 66
• 239000004009 herbicide Substances 0.000 description 45
• 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 description 26
• 125000000229 (C1-C4)alkoxy group Chemical group 0.000 description 23
• 125000004209 (C1-C8) alkyl group Chemical group 0.000 description 19
• 230000002363 herbicidal effect Effects 0.000 description 19
• 125000000623 heterocyclic group Chemical group 0.000 description 17
• 229910052760 oxygen Inorganic materials 0.000 description 17
• YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 16
• 239000000460 chlorine Substances 0.000 description 16
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 16
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 15
• 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 description 14
• DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 14
• 229910052801 chlorine Inorganic materials 0.000 description 14
• 125000001309 chloro group Chemical group Cl* 0.000 description 14
• 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 14
• 239000004215 Carbon black (E152) Substances 0.000 description 13
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 13
• 229930195733 hydrocarbon Natural products 0.000 description 13
• ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 12
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
• 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 11
• 239000001301 oxygen Substances 0.000 description 11
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 11
• 239000002689 soil Substances 0.000 description 11
• 229910052717 sulfur Inorganic materials 0.000 description 11
• QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 10
• 125000005842 heteroatom Chemical group 0.000 description 10
• 230000003313 weakening effect Effects 0.000 description 10
• 235000010469 Glycine max Nutrition 0.000 description 9
• 240000007594 Oryza sativa Species 0.000 description 9
• NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 9
• 235000013339 cereals Nutrition 0.000 description 9
• 229910052731 fluorine Inorganic materials 0.000 description 9
• 230000035784 germination Effects 0.000 description 9
• 239000008187 granular material Substances 0.000 description 9
• 239000011593 sulfur Substances 0.000 description 9
• OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 8
• 235000007164 Oryza sativa Nutrition 0.000 description 8
• 240000008042 Zea mays Species 0.000 description 8
• 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 8
• 235000002017 Zea mays subsp mays Nutrition 0.000 description 8
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 8
• 235000005822 corn Nutrition 0.000 description 8
• 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 8
• QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 8
• 235000009566 rice Nutrition 0.000 description 8
• 238000005507 spraying Methods 0.000 description 8
• 125000001424 substituent group Chemical group 0.000 description 8
• 238000011282 treatment Methods 0.000 description 8
• 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 description 7
• 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 description 7
• 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 description 7
• 244000075850 Avena orientalis Species 0.000 description 7
• 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 7
• 230000000694 effects Effects 0.000 description 7
• 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 7
• 125000002887 hydroxy group Chemical group [H]O* 0.000 description 7
• CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
• 235000007319 Avena orientalis Nutrition 0.000 description 6
• 240000002791 Brassica napus Species 0.000 description 6
• 235000006008 Brassica napus var napus Nutrition 0.000 description 6
• 125000000882 C2-C6 alkenyl group Chemical group 0.000 description 6
• PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 6
• 244000068988 Glycine max Species 0.000 description 6
• 235000011684 Sorghum saccharatum Nutrition 0.000 description 6
• YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
• 229910052799 carbon Inorganic materials 0.000 description 6
• 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 6
• 150000002148 esters Chemical class 0.000 description 6
• 239000011737 fluorine Substances 0.000 description 6
• 239000000843 powder Substances 0.000 description 6
• 125000006413 ring segment Chemical group 0.000 description 6
• 239000011734 sodium Substances 0.000 description 6
• 229910052708 sodium Inorganic materials 0.000 description 6
• SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 description 6
• 125000006648 (C1-C8) haloalkyl group Chemical group 0.000 description 5
• 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 description 5
• 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 5
• 229920000742 Cotton Polymers 0.000 description 5
• 244000299507 Gossypium hirsutum Species 0.000 description 5
• 235000007340 Hordeum vulgare Nutrition 0.000 description 5
• 240000005979 Hordeum vulgare Species 0.000 description 5
• 235000007238 Secale cereale Nutrition 0.000 description 5
• 244000082988 Secale cereale Species 0.000 description 5
• 240000003829 Sorghum propinquum Species 0.000 description 5
• 235000021536 Sugar beet Nutrition 0.000 description 5
• 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 5
• IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 description 5
• JSYGRUBHOCKMGQ-UHFFFAOYSA-N dichloramine Chemical compound ClNCl JSYGRUBHOCKMGQ-UHFFFAOYSA-N 0.000 description 5
• 239000000839 emulsion Substances 0.000 description 5
• 230000012010 growth Effects 0.000 description 5
• 125000004430 oxygen atom Chemical group O* 0.000 description 5
• 239000000575 pesticide Substances 0.000 description 5
• 229920006395 saturated elastomer Polymers 0.000 description 5
• 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 description 4
• 125000004191 (C1-C6) alkoxy group Chemical group 0.000 description 4
• 125000006652 (C3-C12) cycloalkyl group Chemical group 0.000 description 4
• YIVXMZJTEQBPQO-UHFFFAOYSA-N 2,4-DB Chemical compound OC(=O)CCCOC1=CC=C(Cl)C=C1Cl YIVXMZJTEQBPQO-UHFFFAOYSA-N 0.000 description 4
• 239000002794 2,4-DB Substances 0.000 description 4
• OHXLAOJLJWLEIP-UHFFFAOYSA-N 2-(dichloromethyl)-2-methyl-1,3-dioxolane Chemical compound ClC(Cl)C1(C)OCCO1 OHXLAOJLJWLEIP-UHFFFAOYSA-N 0.000 description 4
• IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical compound CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 description 4
• 125000003601 C2-C6 alkynyl group Chemical group 0.000 description 4
• 239000005562 Glyphosate Substances 0.000 description 4
• YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 4
• 240000000111 Saccharum officinarum Species 0.000 description 4
• 235000007201 Saccharum officinarum Nutrition 0.000 description 4
• 241000209140 Triticum Species 0.000 description 4
• 235000021307 Triticum Nutrition 0.000 description 4
• 239000002253 acid Substances 0.000 description 4
• 235000013399 edible fruits Nutrition 0.000 description 4
• 125000002541 furyl group Chemical group 0.000 description 4
• 125000004433 nitrogen atom Chemical group N* 0.000 description 4
• 238000002360 preparation method Methods 0.000 description 4
• 239000011814 protection agent Substances 0.000 description 4
• VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
• 239000002904 solvent Substances 0.000 description 4
• 238000012360 testing method Methods 0.000 description 4
• WMMQJAQJAPXWDO-UHFFFAOYSA-N (4-chlorophenyl) n-methylcarbamate Chemical compound CNC(=O)OC1=CC=C(Cl)C=C1 WMMQJAQJAPXWDO-UHFFFAOYSA-N 0.000 description 3
• 125000004758 (C1-C4) alkoxyimino group Chemical group 0.000 description 3
• 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 description 3
• WNTGYJSOUMFZEP-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-UHFFFAOYSA-N 0.000 description 3
• ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
• WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
• 125000004399 C1-C4 alkenyl group Chemical group 0.000 description 3
• 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 description 3
• 239000005504 Dicamba Substances 0.000 description 3
• 239000005561 Glufosinate Substances 0.000 description 3
• 235000003222 Helianthus annuus Nutrition 0.000 description 3
• XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
• 235000007688 Lycopersicon esculentum Nutrition 0.000 description 3
• 239000005574 MCPA Substances 0.000 description 3
• ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
• KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
• 240000003768 Solanum lycopersicum Species 0.000 description 3
• 235000002595 Solanum tuberosum Nutrition 0.000 description 3
• 244000061456 Solanum tuberosum Species 0.000 description 3
• 240000006694 Stellaria media Species 0.000 description 3
• WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 description 3
• 125000002252 acyl group Chemical group 0.000 description 3
• 229910052783 alkali metal Inorganic materials 0.000 description 3
• MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 description 3
• GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
• 229910052794 bromium Inorganic materials 0.000 description 3
• 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 3
• 239000003974 emollient agent Substances 0.000 description 3
• 239000003995 emulsifying agent Substances 0.000 description 3
• 239000000417 fungicide Substances 0.000 description 3
• XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 description 3
• 229940097068 glyphosate Drugs 0.000 description 3
• 125000004438 haloalkoxy group Chemical group 0.000 description 3
• 229910052500 inorganic mineral Inorganic materials 0.000 description 3
• 239000002917 insecticide Substances 0.000 description 3
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 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 description 3
• 239000002480 mineral oil Substances 0.000 description 3
• 238000002156 mixing Methods 0.000 description 3
• LFGREXWGYUGZLY-UHFFFAOYSA-N phosphoryl Chemical group [P]=O LFGREXWGYUGZLY-UHFFFAOYSA-N 0.000 description 3
• 230000000885 phytotoxic effect Effects 0.000 description 3
• 235000012015 potatoes Nutrition 0.000 description 3
• 239000000243 solution Substances 0.000 description 3
• 238000009331 sowing Methods 0.000 description 3
• YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
• 125000001544 thienyl group Chemical group 0.000 description 3
• SODPIMGUZLOIPE-UHFFFAOYSA-N (4-chlorophenoxy)acetic acid Chemical compound OC(=O)COC1=CC=C(Cl)C=C1 SODPIMGUZLOIPE-UHFFFAOYSA-N 0.000 description 2
• ANDISDKUUWWXKD-UHFFFAOYSA-N (5-chloroquinolin-8-yl) ethaneperoxoate Chemical compound C1=CN=C2C(OOC(=O)C)=CC=C(Cl)C2=C1 ANDISDKUUWWXKD-UHFFFAOYSA-N 0.000 description 2
• 125000006650 (C2-C4) alkynyl group Chemical group 0.000 description 2
• MHULQDZDXMHODA-UHFFFAOYSA-N 1-(2,2-dichloroacetyl)-3,3,8a-trimethyl-2,4,7,8-tetrahydropyrrolo[1,2-a]pyrimidin-6-one Chemical compound C1C(C)(C)CN(C(=O)C(Cl)Cl)C2(C)N1C(=O)CC2 MHULQDZDXMHODA-UHFFFAOYSA-N 0.000 description 2
• XEJNEDVTJPXRSM-UHFFFAOYSA-N 1-(2,4-dichlorophenyl)-5-methyl-4,5-dihydro-1H-pyrazole-3,5-dicarboxylic acid Chemical compound OC(=O)C1(C)CC(C(O)=O)=NN1C1=CC=C(Cl)C=C1Cl XEJNEDVTJPXRSM-UHFFFAOYSA-N 0.000 description 2
• QWWHRELOCZEQNZ-UHFFFAOYSA-N 2,2-dichloro-1-(1-oxa-4-azaspiro[4.5]decan-4-yl)ethanone Chemical compound ClC(Cl)C(=O)N1CCOC11CCCCC1 QWWHRELOCZEQNZ-UHFFFAOYSA-N 0.000 description 2
• MCNOFYBITGAAGM-UHFFFAOYSA-N 2,2-dichloro-1-[5-(furan-2-yl)-2,2-dimethyl-1,3-oxazolidin-3-yl]ethanone Chemical compound C1N(C(=O)C(Cl)Cl)C(C)(C)OC1C1=CC=CO1 MCNOFYBITGAAGM-UHFFFAOYSA-N 0.000 description 2
• OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 2
• AXHCGXRBOHBEQA-UHFFFAOYSA-N 2-(5-chloro-2-methylphenoxy)acetic acid Chemical compound CC1=CC=C(Cl)C=C1OCC(O)=O AXHCGXRBOHBEQA-UHFFFAOYSA-N 0.000 description 2
• LLWADFLAOKUBDR-UHFFFAOYSA-N 2-methyl-4-chlorophenoxybutyric acid Chemical compound CC1=CC(Cl)=CC=C1OCCCC(O)=O LLWADFLAOKUBDR-UHFFFAOYSA-N 0.000 description 2
• CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical compound O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 description 2
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