KR20090024120A - 제초성 혼합물 - Google Patents

Info

Publication number

KR20090024120A

KR20090024120A KR1020087027364A KR20087027364A KR20090024120A KR 20090024120 A KR20090024120 A KR 20090024120A KR 1020087027364 A KR1020087027364 A KR 1020087027364A KR 20087027364 A KR20087027364 A KR 20087027364A KR 20090024120 A KR20090024120 A KR 20090024120A

Authority

KR

South Korea

Prior art keywords

compound

methyl

mixture

amino

cyclopropyl

Prior art date

2006-04-10

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

Links

• Espacenet
• Global Dossier
• Discuss

• 239000000203 mixture Substances 0.000 title claims abstract description 301
• 230000002363 herbicidal effect Effects 0.000 title claims abstract description 181
• 150000001875 compounds Chemical class 0.000 claims abstract description 413
• 239000004009 herbicide Substances 0.000 claims abstract description 176
• -1 cinnamline Chemical compound 0.000 claims abstract description 97
• 239000003112 inhibitor Substances 0.000 claims abstract description 66
• 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 abstract description 61
• GRSMWKLPSNHDHA-UHFFFAOYSA-N Naphthalic anhydride Chemical compound C1=CC(C(=O)OC2=O)=C3C2=CC=CC3=C1 GRSMWKLPSNHDHA-UHFFFAOYSA-N 0.000 claims abstract description 36
• 238000000034 method Methods 0.000 claims abstract description 33
• 230000012010 growth Effects 0.000 claims abstract description 27
• 150000003839 salts Chemical class 0.000 claims abstract description 23
• 125000000217 alkyl group Chemical group 0.000 claims abstract description 15
• 108010060806 Photosystem II Protein Complex Proteins 0.000 claims abstract description 14
• SEOVTRFCIGRIMH-UHFFFAOYSA-N indole-3-acetic acid Chemical class C1=CC=C2C(CC(=O)O)=CNC2=C1 SEOVTRFCIGRIMH-UHFFFAOYSA-N 0.000 claims abstract description 13
• 150000004669 very long chain fatty acids Chemical class 0.000 claims abstract description 11
• 150000001204 N-oxides Chemical class 0.000 claims abstract description 9
• 125000004183 alkoxy alkyl group Chemical group 0.000 claims abstract description 9
• 125000005081 alkoxyalkoxyalkyl group Chemical group 0.000 claims abstract description 9
• 229930192334 Auxin Natural products 0.000 claims abstract description 8
• 108010081996 Photosystem I Protein Complex Proteins 0.000 claims abstract description 8
• 239000002363 auxin Substances 0.000 claims abstract description 8
• 239000003795 chemical substances by application Substances 0.000 claims abstract description 8
• 125000002768 hydroxyalkyl group Chemical group 0.000 claims abstract description 8
• 229910052799 carbon Inorganic materials 0.000 claims abstract description 7
• 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 7
• BWPYBAJTDILQPY-UHFFFAOYSA-N Methoxyphenone Chemical compound C1=C(C)C(OC)=CC=C1C(=O)C1=CC=CC(C)=C1 BWPYBAJTDILQPY-UHFFFAOYSA-N 0.000 claims abstract description 6
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 6
• AHXUVTKVCMOKIX-UHFFFAOYSA-N 1-bromo-4-(chloromethylsulfonyl)benzene Chemical compound ClCS(=O)(=O)C1=CC=C(Br)C=C1 AHXUVTKVCMOKIX-UHFFFAOYSA-N 0.000 claims abstract description 5
• OHXLAOJLJWLEIP-UHFFFAOYSA-N 2-(dichloromethyl)-2-methyl-1,3-dioxolane Chemical compound ClC(Cl)C1(C)OCCO1 OHXLAOJLJWLEIP-UHFFFAOYSA-N 0.000 claims abstract description 5
• PFJJMJDEVDLPNE-UHFFFAOYSA-N Benoxacor Chemical compound C1=CC=C2N(C(=O)C(Cl)Cl)C(C)COC2=C1 PFJJMJDEVDLPNE-UHFFFAOYSA-N 0.000 claims abstract description 5
• GMBRUAIJEFRHFQ-UHFFFAOYSA-N Fenchlorazole-ethyl Chemical group N1=C(C(=O)OCC)N=C(C(Cl)(Cl)Cl)N1C1=CC=C(Cl)C=C1Cl GMBRUAIJEFRHFQ-UHFFFAOYSA-N 0.000 claims abstract description 5
• 239000004606 Fillers/Extenders Substances 0.000 claims abstract description 5
• 239000002253 acid Substances 0.000 claims abstract description 5
• 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 abstract description 5
• 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims abstract description 5
• 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 abstract description 5
• WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims abstract description 4
• LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims abstract description 4
• QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims abstract description 4
• 239000005644 Dazomet Substances 0.000 claims abstract description 4
• ICWUMLXQKFTJMH-UHFFFAOYSA-N Etobenzanid Chemical compound C1=CC(OCOCC)=CC=C1C(=O)NC1=CC=CC(Cl)=C1Cl ICWUMLXQKFTJMH-UHFFFAOYSA-N 0.000 claims abstract description 4
• GXAMYUGOODKVRM-UHFFFAOYSA-N Flurecol Chemical compound C1=CC=C2C(C(=O)O)(O)C3=CC=CC=C3C2=C1 GXAMYUGOODKVRM-UHFFFAOYSA-N 0.000 claims abstract description 4
• UKSLKNUCVPZQCQ-UHFFFAOYSA-N Fluxofenim Chemical compound C=1C=C(Cl)C=CC=1C(C(F)(F)F)=NOCC1OCCO1 UKSLKNUCVPZQCQ-UHFFFAOYSA-N 0.000 claims abstract description 4
• 239000005642 Oleic acid Substances 0.000 claims abstract description 4
• ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims abstract description 4
• 208000014347 autosomal dominant hyaline body myopathy Diseases 0.000 claims abstract description 4
• 229910052794 bromium Inorganic materials 0.000 claims abstract description 4
• WZDDLAZXUYIVMU-UHFFFAOYSA-N bromobutide Chemical compound CC(C)(C)C(Br)C(=O)NC(C)(C)C1=CC=CC=C1 WZDDLAZXUYIVMU-UHFFFAOYSA-N 0.000 claims abstract description 4
• QAYICIQNSGETAS-UHFFFAOYSA-N dazomet Chemical compound CN1CSC(=S)N(C)C1 QAYICIQNSGETAS-UHFFFAOYSA-N 0.000 claims abstract description 4
• 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 abstract description 4
• SDIXRDNYIMOKSG-UHFFFAOYSA-L disodium methyl arsenate Chemical compound [Na+].[Na+].C[As]([O-])([O-])=O SDIXRDNYIMOKSG-UHFFFAOYSA-L 0.000 claims abstract description 4
• QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims abstract description 4
• RBNIGDFIUWJJEV-LLVKDONJSA-N methyl (2r)-2-(n-benzoyl-3-chloro-4-fluoroanilino)propanoate Chemical group C=1C=C(F)C(Cl)=CC=1N([C@H](C)C(=O)OC)C(=O)C1=CC=CC=C1 RBNIGDFIUWJJEV-LLVKDONJSA-N 0.000 claims abstract description 4
• JITOKQVGRJSHHA-UHFFFAOYSA-M monosodium methyl arsenate Chemical compound [Na+].C[As](O)([O-])=O JITOKQVGRJSHHA-UHFFFAOYSA-M 0.000 claims abstract description 4
• ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims abstract description 4
• IKVXBIIHQGXQRQ-CYBMUJFWSA-N propan-2-yl (2r)-2-(n-benzoyl-3-chloro-4-fluoroanilino)propanoate Chemical group C=1C=C(F)C(Cl)=CC=1N([C@H](C)C(=O)OC(C)C)C(=O)C1=CC=CC=C1 IKVXBIIHQGXQRQ-CYBMUJFWSA-N 0.000 claims abstract description 4
• 150000003230 pyrimidines Chemical class 0.000 claims abstract description 4
• 125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 claims 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 claims abstract description 3
• 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims abstract description 3
• AFCCDDWKHLHPDF-UHFFFAOYSA-M metam-sodium Chemical compound [Na+].CNC([S-])=S AFCCDDWKHLHPDF-UHFFFAOYSA-M 0.000 claims abstract 2
• PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 95
• 239000005562 Glyphosate Substances 0.000 claims description 68
• 229940097068 glyphosate Drugs 0.000 claims description 49
• XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims description 49
• 239000005623 Thifensulfuron-methyl Substances 0.000 claims description 48
• MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 claims description 48
• AHTPATJNIAFOLR-UHFFFAOYSA-N thifensulfuron-methyl Chemical group S1C=CC(S(=O)(=O)NC(=O)NC=2N=C(OC)N=C(C)N=2)=C1C(=O)OC AHTPATJNIAFOLR-UHFFFAOYSA-N 0.000 claims description 48
• 239000005560 Foramsulfuron Substances 0.000 claims description 47
• PXDNXJSDGQBLKS-UHFFFAOYSA-N foramsulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=C(NC=O)C=2)C(=O)N(C)C)=N1 PXDNXJSDGQBLKS-UHFFFAOYSA-N 0.000 claims description 47
• 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 claims description 44
• IRJQWZWMQCVOLA-ZBKNUEDVSA-N 2-[(z)-n-[(3,5-difluorophenyl)carbamoylamino]-c-methylcarbonimidoyl]pyridine-3-carboxylic acid Chemical compound N=1C=CC=C(C(O)=O)C=1C(/C)=N\NC(=O)NC1=CC(F)=CC(F)=C1 IRJQWZWMQCVOLA-ZBKNUEDVSA-N 0.000 claims description 34
• 239000005617 S-Metolachlor Substances 0.000 claims description 34
• YMXOXAPKZDWXLY-QWRGUYRKSA-N tribenuron methyl Chemical group COC(=O)[C@H]1CCCC[C@@H]1S(=O)(=O)NC(=O)N(C)C1=NC(C)=NC(OC)=N1 YMXOXAPKZDWXLY-QWRGUYRKSA-N 0.000 claims description 33
• 239000005616 Rimsulfuron Substances 0.000 claims description 30
• MEFOUWRMVYJCQC-UHFFFAOYSA-N rimsulfuron Chemical compound CCS(=O)(=O)C1=CC=CN=C1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 MEFOUWRMVYJCQC-UHFFFAOYSA-N 0.000 claims description 30
• WVQBLGZPHOPPFO-LBPRGKRZSA-N (S)-metolachlor Chemical compound CCC1=CC=CC(C)=C1N([C@@H](C)COC)C(=O)CCl WVQBLGZPHOPPFO-LBPRGKRZSA-N 0.000 claims description 29
• XMTQQYYKAHVGBJ-UHFFFAOYSA-N 3-(3,4-DICHLOROPHENYL)-1,1-DIMETHYLUREA Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XMTQQYYKAHVGBJ-UHFFFAOYSA-N 0.000 claims description 27
• 239000005510 Diuron Substances 0.000 claims description 27
• 239000005586 Nicosulfuron Substances 0.000 claims description 26
• RTCOGUMHFFWOJV-UHFFFAOYSA-N nicosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CN=2)C(=O)N(C)C)=N1 RTCOGUMHFFWOJV-UHFFFAOYSA-N 0.000 claims description 26
• 239000005561 Glufosinate Substances 0.000 claims description 25
• FIKAKWIAUPDISJ-UHFFFAOYSA-L paraquat dichloride Chemical compound [Cl-].[Cl-].C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 FIKAKWIAUPDISJ-UHFFFAOYSA-L 0.000 claims description 25
• YHKBGVDUSSWOAB-UHFFFAOYSA-N 2-chloro-3-{2-chloro-5-[4-(difluoromethyl)-3-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]-4-fluorophenyl}propanoic acid Chemical compound O=C1N(C(F)F)C(C)=NN1C1=CC(CC(Cl)C(O)=O)=C(Cl)C=C1F YHKBGVDUSSWOAB-UHFFFAOYSA-N 0.000 claims description 22
• 239000005532 Flumioxazine Substances 0.000 claims description 21
• 239000005590 Oxyfluorfen Substances 0.000 claims description 21
• OQMBBFQZGJFLBU-UHFFFAOYSA-N Oxyfluorfen Chemical compound C1=C([N+]([O-])=O)C(OCC)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 OQMBBFQZGJFLBU-UHFFFAOYSA-N 0.000 claims description 21
• 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 claims description 21
• OORLZFUTLGXMEF-UHFFFAOYSA-N sulfentrazone Chemical compound O=C1N(C(F)F)C(C)=NN1C1=CC(NS(C)(=O)=O)=C(Cl)C=C1Cl OORLZFUTLGXMEF-UHFFFAOYSA-N 0.000 claims description 21
• WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 claims description 20
• 239000003085 diluting agent Substances 0.000 claims description 15
• 239000004094 surface-active agent Substances 0.000 claims description 15
• 108010000700 Acetolactate synthase Proteins 0.000 claims description 12
• 102000005396 glutamine synthetase Human genes 0.000 claims description 11
• 108020002326 glutamine synthetase Proteins 0.000 claims description 11
• 102000000452 Acetyl-CoA carboxylase Human genes 0.000 claims description 9
• 108010016219 Acetyl-CoA carboxylase Proteins 0.000 claims description 9
• 239000007788 liquid Substances 0.000 claims description 9
• 239000007787 solid Substances 0.000 claims description 7
• 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 claims description 6
• KWAIHLIXESXTJL-UHFFFAOYSA-N aminocyclopyrachlor Chemical compound OC(=O)C1=C(Cl)C(N)=NC(C2CC2)=N1 KWAIHLIXESXTJL-UHFFFAOYSA-N 0.000 claims description 6
• MDWRNPOBHVLALB-UHFFFAOYSA-N aminocyclopyrachlor-methyl Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C2CC2)=N1 MDWRNPOBHVLALB-UHFFFAOYSA-N 0.000 claims description 6
• 239000000080 wetting agent Substances 0.000 claims description 6
• 102000003960 Ligases Human genes 0.000 claims description 5
• 108090000364 Ligases Proteins 0.000 claims description 5
• 102000004316 Oxidoreductases Human genes 0.000 claims description 5
• 108090000854 Oxidoreductases Proteins 0.000 claims description 5
• 229910019142 PO4 Inorganic materials 0.000 claims description 4
• 239000010452 phosphate Substances 0.000 claims description 4
• BJQDYHYTWDPPIV-UHFFFAOYSA-N 1-butoxypropan-2-yl 6-amino-5-chloro-2-cyclopropylpyrimidine-4-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC(C)COCCCC)=NC(C2CC2)=N1 BJQDYHYTWDPPIV-UHFFFAOYSA-N 0.000 claims description 3
• DYSFDPGVHAGPBC-UHFFFAOYSA-N 2-butoxyethyl 6-amino-5-chloro-2-cyclopropylpyrimidine-4-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OCCOCCCC)=NC(C2CC2)=N1 DYSFDPGVHAGPBC-UHFFFAOYSA-N 0.000 claims description 3
• QDMHMEDHEMXGLO-UHFFFAOYSA-N 2-ethylhexyl 6-amino-5-chloro-2-cyclopropylpyrimidine-4-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OCC(CC)CCCC)=NC(C2CC2)=N1 QDMHMEDHEMXGLO-UHFFFAOYSA-N 0.000 claims description 3
• RROBAZRVYTZHGX-UHFFFAOYSA-N 3-hydroxypropyl 6-amino-5-chloro-2-cyclopropylpyrimidine-4-carboxylate Chemical compound OCCCOC(=O)C1=C(Cl)C(N)=NC(C2CC2)=N1 RROBAZRVYTZHGX-UHFFFAOYSA-N 0.000 claims description 3
• BTUSKWROSWXMPG-UHFFFAOYSA-N 6-amino-2-(4-bromophenyl)-5-chloropyrimidine-4-carboxylic acid Chemical compound OC(=O)C1=C(Cl)C(N)=NC(C=2C=CC(Br)=CC=2)=N1 BTUSKWROSWXMPG-UHFFFAOYSA-N 0.000 claims description 3
• DWIDAOMPDCVMCY-UHFFFAOYSA-N 6-amino-5-bromo-2-cyclopropylpyrimidine-4-carboxylic acid Chemical compound OC(=O)C1=C(Br)C(N)=NC(C2CC2)=N1 DWIDAOMPDCVMCY-UHFFFAOYSA-N 0.000 claims description 3
• IFNGRCNEIXJJOA-UHFFFAOYSA-N 6-amino-5-chloro-2-(4-chlorophenyl)pyrimidine-4-carboxylic acid Chemical compound OC(=O)C1=C(Cl)C(N)=NC(C=2C=CC(Cl)=CC=2)=N1 IFNGRCNEIXJJOA-UHFFFAOYSA-N 0.000 claims description 3
• GKGQGHXICXHRDC-UHFFFAOYSA-N benzyl 6-amino-5-bromo-2-cyclopropylpyrimidine-4-carboxylate Chemical compound BrC=1C(N)=NC(C2CC2)=NC=1C(=O)OCC1=CC=CC=C1 GKGQGHXICXHRDC-UHFFFAOYSA-N 0.000 claims description 3
• PLSRLZJGTQNHJW-UHFFFAOYSA-N benzyl 6-amino-5-chloro-2-cyclopropylpyrimidine-4-carboxylate Chemical compound ClC=1C(N)=NC(C2CC2)=NC=1C(=O)OCC1=CC=CC=C1 PLSRLZJGTQNHJW-UHFFFAOYSA-N 0.000 claims description 3
• QRIQBFGOPOEBBT-UHFFFAOYSA-N butyl 6-amino-5-chloro-2-cyclopropylpyrimidine-4-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OCCCC)=NC(C2CC2)=N1 QRIQBFGOPOEBBT-UHFFFAOYSA-N 0.000 claims description 3
• ASZOFVYKIHWIRJ-UHFFFAOYSA-N ethyl 6-amino-2-(4-bromophenyl)-5-chloropyrimidine-4-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OCC)=NC(C=2C=CC(Br)=CC=2)=N1 ASZOFVYKIHWIRJ-UHFFFAOYSA-N 0.000 claims description 3
• DFNPYOBOAGIMIV-UHFFFAOYSA-N ethyl 6-amino-5-bromo-2-cyclopropylpyrimidine-4-carboxylate Chemical compound NC1=C(Br)C(C(=O)OCC)=NC(C2CC2)=N1 DFNPYOBOAGIMIV-UHFFFAOYSA-N 0.000 claims description 3
• PXCZEJRHVNHLHI-UHFFFAOYSA-N ethyl 6-amino-5-chloro-2-(4-chlorophenyl)pyrimidine-4-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OCC)=NC(C=2C=CC(Cl)=CC=2)=N1 PXCZEJRHVNHLHI-UHFFFAOYSA-N 0.000 claims description 3
• NMPOJZJYKCNZDZ-UHFFFAOYSA-N ethyl 6-amino-5-chloro-2-cyclopropylpyrimidine-4-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OCC)=NC(C2CC2)=N1 NMPOJZJYKCNZDZ-UHFFFAOYSA-N 0.000 claims description 3
• RDTDHIKLTPWILZ-UHFFFAOYSA-N methyl 6-amino-2-(4-bromophenyl)-5-chloropyrimidine-4-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C=CC(Br)=CC=2)=N1 RDTDHIKLTPWILZ-UHFFFAOYSA-N 0.000 claims description 3
• YDLGIPUCLCBOMQ-UHFFFAOYSA-N methyl 6-amino-5-bromo-2-cyclopropylpyrimidine-4-carboxylate Chemical compound NC1=C(Br)C(C(=O)OC)=NC(C2CC2)=N1 YDLGIPUCLCBOMQ-UHFFFAOYSA-N 0.000 claims description 3
• NRMIASFSJMZYBG-UHFFFAOYSA-N methyl 6-amino-5-chloro-2-(4-chlorophenyl)pyrimidine-4-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC)=NC(C=2C=CC(Cl)=CC=2)=N1 NRMIASFSJMZYBG-UHFFFAOYSA-N 0.000 claims description 3
• KLGNDEBQUZCJDW-UHFFFAOYSA-N octan-2-yl 6-amino-5-chloro-2-cyclopropylpyrimidine-4-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC(C)CCCCCC)=NC(C2CC2)=N1 KLGNDEBQUZCJDW-UHFFFAOYSA-N 0.000 claims description 3
• XJVFEPYNJCZLSU-UHFFFAOYSA-N octyl 6-amino-5-chloro-2-cyclopropylpyrimidine-4-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OCCCCCCCC)=NC(C2CC2)=N1 XJVFEPYNJCZLSU-UHFFFAOYSA-N 0.000 claims description 3
• MOLCPAFIBVEELG-UHFFFAOYSA-N propan-2-yl 6-amino-5-chloro-2-cyclopropylpyrimidine-4-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OC(C)C)=NC(C2CC2)=N1 MOLCPAFIBVEELG-UHFFFAOYSA-N 0.000 claims description 3
• ZUTZYQPFLDQYDL-UHFFFAOYSA-N propyl 6-amino-5-chloro-2-cyclopropylpyrimidine-4-carboxylate Chemical compound NC1=C(Cl)C(C(=O)OCCC)=NC(C2CC2)=N1 ZUTZYQPFLDQYDL-UHFFFAOYSA-N 0.000 claims description 3
• GQVOXSBHXPZQSS-UHFFFAOYSA-M sodium;6-amino-5-bromo-2-cyclopropylpyrimidine-4-carboxylate Chemical compound [Na+].[O-]C(=O)C1=C(Br)C(N)=NC(C2CC2)=N1 GQVOXSBHXPZQSS-UHFFFAOYSA-M 0.000 claims description 3
• CYILDCWNUWUWEG-UHFFFAOYSA-M sodium;6-amino-5-chloro-2-cyclopropylpyrimidine-4-carboxylate Chemical compound [Na+].[O-]C(=O)C1=C(Cl)C(N)=NC(C2CC2)=N1 CYILDCWNUWUWEG-UHFFFAOYSA-M 0.000 claims description 3
• 235000012054 meals Nutrition 0.000 claims description 2
• 239000003053 toxin Substances 0.000 claims description 2
• 231100000765 toxin Toxicity 0.000 claims description 2
• 239000005574 MCPA Substances 0.000 claims 1
• 108010020183 3-phosphoshikimate 1-carboxyvinyltransferase Proteins 0.000 abstract description 4
• 239000005499 Clomazone Substances 0.000 abstract description 3
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