AR109100A1 - Composiciones herbicidas que comprenden fenilpirimidinas - Google Patents
Composiciones herbicidas que comprenden fenilpirimidinasInfo
- Publication number
- AR109100A1 AR109100A1 ARP170102021A ARP170102021A AR109100A1 AR 109100 A1 AR109100 A1 AR 109100A1 AR P170102021 A ARP170102021 A AR P170102021A AR P170102021 A ARP170102021 A AR P170102021A AR 109100 A1 AR109100 A1 AR 109100A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- carbonyl
- haloalkoxy
- haloalkylthio
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title abstract 6
- 239000000203 mixture Substances 0.000 title abstract 5
- 230000002363 herbicidal effect Effects 0.000 title abstract 3
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 57
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 17
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 17
- 239000003112 inhibitor Substances 0.000 abstract 15
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 15
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 14
- -1 C2−6-haloalkenyl Chemical group 0.000 abstract 14
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 12
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 10
- 229910052736 halogen Inorganic materials 0.000 abstract 9
- 150000002367 halogens Chemical group 0.000 abstract 9
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 9
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 abstract 7
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 6
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 5
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 4
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- 150000003839 salts Chemical class 0.000 abstract 4
- 125000001424 substituent group Chemical group 0.000 abstract 4
- 125000001072 heteroaryl group Chemical group 0.000 abstract 3
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 abstract 3
- 125000006296 sulfonyl amino group Chemical group [H]N(*)S(*)(=O)=O 0.000 abstract 3
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 abstract 3
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 2
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 2
- OTSAMNSACVKIOJ-UHFFFAOYSA-N azane;carbamoyl(ethoxy)phosphinic acid Chemical compound [NH4+].CCOP([O-])(=O)C(N)=O OTSAMNSACVKIOJ-UHFFFAOYSA-N 0.000 abstract 2
- 230000015572 biosynthetic process Effects 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical group O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 abstract 2
- 150000004669 very long chain fatty acids Chemical class 0.000 abstract 2
- GXEKYRXVRROBEV-FBXFSONDSA-N (1r,2s,3r,4s)-7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid Chemical compound C1C[C@@H]2[C@@H](C(O)=O)[C@@H](C(=O)O)[C@H]1O2 GXEKYRXVRROBEV-FBXFSONDSA-N 0.000 abstract 1
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 abstract 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 abstract 1
- SVOAUHHKPGKPQK-UHFFFAOYSA-N 2-chloro-9-hydroxyfluorene-9-carboxylic acid Chemical compound C1=C(Cl)C=C2C(C(=O)O)(O)C3=CC=CC=C3C2=C1 SVOAUHHKPGKPQK-UHFFFAOYSA-N 0.000 abstract 1
- OXPDQFOKSZYEMJ-UHFFFAOYSA-N 2-phenylpyrimidine Chemical compound C1=CC=CC=C1C1=NC=CC=N1 OXPDQFOKSZYEMJ-UHFFFAOYSA-N 0.000 abstract 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 abstract 1
- QUTYKIXIUDQOLK-PRJMDXOYSA-N 5-O-(1-carboxyvinyl)-3-phosphoshikimic acid Chemical compound O[C@H]1[C@H](OC(=C)C(O)=O)CC(C(O)=O)=C[C@H]1OP(O)(O)=O QUTYKIXIUDQOLK-PRJMDXOYSA-N 0.000 abstract 1
- OPEJGICLTMWFNQ-UHFFFAOYSA-N 5-[(2,6-difluorophenyl)methoxymethyl]-5-methyl-3-(3-methylthiophen-2-yl)-4h-1,2-oxazole Chemical compound C1=CSC(C=2CC(C)(COCC=3C(=CC=CC=3F)F)ON=2)=C1C OPEJGICLTMWFNQ-UHFFFAOYSA-N 0.000 abstract 1
- GZJVZGUUTYWVTP-UHFFFAOYSA-N 6-chloro-3-(2-cyclopropyl-6-methylphenoxy)-1h-pyridazin-4-one Chemical compound N=1N=C(Cl)C=C(O)C=1OC=1C(C)=CC=CC=1C1CC1 GZJVZGUUTYWVTP-UHFFFAOYSA-N 0.000 abstract 1
- WBFYVDCHGVNRBH-UHFFFAOYSA-N 7,8-dihydropteroic acid Chemical compound N=1C=2C(=O)NC(N)=NC=2NCC=1CNC1=CC=C(C(O)=O)C=C1 WBFYVDCHGVNRBH-UHFFFAOYSA-N 0.000 abstract 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 abstract 1
- 108010000700 Acetolactate synthase Proteins 0.000 abstract 1
- 229930192334 Auxin Natural products 0.000 abstract 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 abstract 1
- 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 1
- NDUPDOJHUQKPAG-UHFFFAOYSA-N Dalapon Chemical compound CC(Cl)(Cl)C(O)=O NDUPDOJHUQKPAG-UHFFFAOYSA-N 0.000 abstract 1
- 239000005644 Dazomet Substances 0.000 abstract 1
- PHVNLLCAQHGNKU-UHFFFAOYSA-N Dimethipin Chemical compound CC1=C(C)S(=O)(=O)CCS1(=O)=O PHVNLLCAQHGNKU-UHFFFAOYSA-N 0.000 abstract 1
- ICWUMLXQKFTJMH-UHFFFAOYSA-N Etobenzanid Chemical compound C1=CC(OCOCC)=CC=C1C(=O)NC1=CC=CC(Cl)=C1Cl ICWUMLXQKFTJMH-UHFFFAOYSA-N 0.000 abstract 1
- GXAMYUGOODKVRM-UHFFFAOYSA-N Flurecol Chemical compound C1=CC=C2C(C(=O)O)(O)C3=CC=CC=C3C2=C1 GXAMYUGOODKVRM-UHFFFAOYSA-N 0.000 abstract 1
- VEVZCONIUDBCDC-UHFFFAOYSA-N Flurprimidol Chemical compound C=1N=CN=CC=1C(O)(C(C)C)C1=CC=C(OC(F)(F)F)C=C1 VEVZCONIUDBCDC-UHFFFAOYSA-N 0.000 abstract 1
- 239000005983 Maleic hydrazide Substances 0.000 abstract 1
- BGRDGMRNKXEXQD-UHFFFAOYSA-N Maleic hydrazide Chemical compound OC1=CC=C(O)N=N1 BGRDGMRNKXEXQD-UHFFFAOYSA-N 0.000 abstract 1
- OKIBNKKYNPBDRS-UHFFFAOYSA-N Mefluidide Chemical compound CC(=O)NC1=CC(NS(=O)(=O)C(F)(F)F)=C(C)C=C1C OKIBNKKYNPBDRS-UHFFFAOYSA-N 0.000 abstract 1
- 239000002169 Metam Substances 0.000 abstract 1
- FMINYZXVCTYSNY-UHFFFAOYSA-N Methyldymron Chemical compound C=1C=CC=CC=1N(C)C(=O)NC(C)(C)C1=CC=CC=C1 FMINYZXVCTYSNY-UHFFFAOYSA-N 0.000 abstract 1
- IUFUITYPUYMIHI-UHFFFAOYSA-N N-[1-(3,5-dimethylphenoxy)propan-2-yl]-6-(2-fluoropropan-2-yl)-1,3,5-triazine-2,4-diamine Chemical compound N=1C(N)=NC(C(C)(C)F)=NC=1NC(C)COC1=CC(C)=CC(C)=C1 IUFUITYPUYMIHI-UHFFFAOYSA-N 0.000 abstract 1
- 239000005642 Oleic acid Substances 0.000 abstract 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 abstract 1
- 229910019142 PO4 Inorganic materials 0.000 abstract 1
- 239000005643 Pelargonic acid Substances 0.000 abstract 1
- 108020001991 Protoporphyrinogen Oxidase Proteins 0.000 abstract 1
- 102000005135 Protoporphyrinogen oxidase Human genes 0.000 abstract 1
- OBLNWSCLAYSJJR-UHFFFAOYSA-N Quinoclamin Chemical compound C1=CC=C2C(=O)C(N)=C(Cl)C(=O)C2=C1 OBLNWSCLAYSJJR-UHFFFAOYSA-N 0.000 abstract 1
- 239000002167 Quinoclamine Substances 0.000 abstract 1
- IBZHOAONZVJLOB-UHFFFAOYSA-N Tridiphane Chemical compound ClC1=CC(Cl)=CC(C2(CC(Cl)(Cl)Cl)OC2)=C1 IBZHOAONZVJLOB-UHFFFAOYSA-N 0.000 abstract 1
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 208000014347 autosomal dominant hyaline body myopathy Diseases 0.000 abstract 1
- 239000002363 auxin Substances 0.000 abstract 1
- 238000004061 bleaching Methods 0.000 abstract 1
- 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 abstract 1
- PSGPXWYGJGGEEG-UHFFFAOYSA-N butyl 9-hydroxyfluorene-9-carboxylate Chemical group C1=CC=C2C(C(=O)OCCCC)(O)C3=CC=CC=C3C2=C1 PSGPXWYGJGGEEG-UHFFFAOYSA-N 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 230000008166 cellulose biosynthesis Effects 0.000 abstract 1
- QAYICIQNSGETAS-UHFFFAOYSA-N dazomet Chemical compound CN1CSC(=S)N(C)C1 QAYICIQNSGETAS-UHFFFAOYSA-N 0.000 abstract 1
- SDIXRDNYIMOKSG-UHFFFAOYSA-L disodium methyl arsenate Chemical compound [Na+].[Na+].C[As]([O-])([O-])=O SDIXRDNYIMOKSG-UHFFFAOYSA-L 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- QMTNOLKHSWIQBE-FGTMMUONSA-N exo-(+)-cinmethylin Chemical compound O([C@H]1[C@]2(C)CC[C@@](O2)(C1)C(C)C)CC1=CC=CC=C1C QMTNOLKHSWIQBE-FGTMMUONSA-N 0.000 abstract 1
- 102000005396 glutamine synthetase Human genes 0.000 abstract 1
- 108020002326 glutamine synthetase Proteins 0.000 abstract 1
- 125000004995 haloalkylthio group Chemical group 0.000 abstract 1
- YFONKFDEZLYQDH-BOURZNODSA-N indaziflam Chemical compound CC(F)C1=NC(N)=NC(N[C@H]2C3=CC(C)=CC=C3C[C@@H]2C)=N1 YFONKFDEZLYQDH-BOURZNODSA-N 0.000 abstract 1
- SEOVTRFCIGRIMH-UHFFFAOYSA-N indole-3-acetic acid Chemical compound C1=CC=C2C(CC(=O)O)=CNC2=C1 SEOVTRFCIGRIMH-UHFFFAOYSA-N 0.000 abstract 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 abstract 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 150000002632 lipids Chemical class 0.000 abstract 1
- HYVVJDQGXFXBRZ-UHFFFAOYSA-N metam Chemical compound CNC(S)=S HYVVJDQGXFXBRZ-UHFFFAOYSA-N 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- 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 abstract 1
- RBNIGDFIUWJJEV-UHFFFAOYSA-N methyl 2-(n-benzoyl-3-chloro-4-fluoroanilino)propanoate Chemical group C=1C=C(F)C(Cl)=CC=1N(C(C)C(=O)OC)C(=O)C1=CC=CC=C1 RBNIGDFIUWJJEV-UHFFFAOYSA-N 0.000 abstract 1
- LINPVWIEWJTEEJ-UHFFFAOYSA-N methyl 2-chloro-9-hydroxyfluorene-9-carboxylate Chemical group C1=C(Cl)C=C2C(C(=O)OC)(O)C3=CC=CC=C3C2=C1 LINPVWIEWJTEEJ-UHFFFAOYSA-N 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 230000011278 mitosis Effects 0.000 abstract 1
- JITOKQVGRJSHHA-UHFFFAOYSA-M monosodium methyl arsenate Chemical compound [Na+].C[As](O)([O-])=O JITOKQVGRJSHHA-UHFFFAOYSA-M 0.000 abstract 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 abstract 1
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 239000010452 phosphate Substances 0.000 abstract 1
- 230000029553 photosynthesis Effects 0.000 abstract 1
- 238000010672 photosynthesis Methods 0.000 abstract 1
- 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 abstract 1
- VTRWMTJQBQJKQH-UHFFFAOYSA-N pyributicarb Chemical compound COC1=CC=CC(N(C)C(=S)OC=2C=C(C=CC=2)C(C)(C)C)=N1 VTRWMTJQBQJKQH-UHFFFAOYSA-N 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/32—Ingredients for reducing the noxious effect of the active substances to organisms other than pests, e.g. toxicity reducing compositions, self-destructing compositions
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/26—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/08—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing solids as carriers or diluents
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Reivindicación 1: Una composición herbicida caracterizada porque comprende A) al menos una fenilpirimidina de la fórmula (1), en donde en la fórmula (1) las variables tienen los siguientes significados: R¹ es C₁₋₆-alquilo, C₁₋₆-haloalquilo, hidroxi-C₁₋₆-alquilo, C₂₋₆-alquenilo, C₂₋₆-haloalquenilo, C₂₋₆-alquinilo, C₃₋₆-haloalquinilo, C₁₋₆-alcoxi-C₁₋₆-alquilo, C₁₋₆-alcoxi, C₃₋₆-alqueniloxi, C₃₋₆-haloalqueniloxi, C₃₋₆-alquiniloxi, C₃₋₆-haloalquiniloxi, C₁₋₆-haloalcoxi, C₃₋₆-cicloalcoxi, C₃₋₆-halocicloalcoxi, C₃₋₆-cicloalqueniloxi, C₃₋₆-halocicloalqueniloxi, C₁₋₆-alquiltio, C₁₋₆-haloalquiltio, (C₁₋₆-alquil)amino, di(C₁₋₆-alquil)amino, C₁₋₆-alquilsulfinilo, C₁₋₆-alquilsulfonilo, C₃₋₆-cicloalquilo, C₃₋₆-cicloalquenilo, C₃₋₆-halocicloalquilo, C₃₋₆-halocicloalquenilo, [1-(C₁₋₆-alquil)]-C₃₋₆-cicloalquilo, [1-(C₂₋₆-alquenil)]-C₃₋₆-cicloalquilo, [1-(C₂₋₆-alquinil)]-C₃₋₆-cicloalquilo, [1-(C₁₋₆-haloalquil)]-C₃₋₆-cicloalquilo, [1-(C₂₋₆-haloalquenil)]-C₃₋₆-cicloalquilo, [1-(C₃₋₆-haloalquinil)]-C₃₋₆-cicloalquilo, C₃₋₆-cicloalquil-C₁₋₆-alquilo, C₃₋₆-cicloalquil-C₁₋₆-haloalquilo, C₃₋₆-cicloalquil-C₁₋₆-alcoxi, C₃₋₆-cicloalquil-C₁₋₆-haloalcoxi, fenilo, heteroarilo de 5 ó 6 miembros, o heterociclilo de 3 a 6 miembros en donde los sustituyentes de cicloalquilo, fenilo, heteroarilo y heterociclilo, independientemente entre sí, son no sustituidos o sustituidos con 1 a 5 sustituyentes seleccionados del grupo que consiste en halógeno, CN, NO₂, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₁₋₆-alcoxi o C₁₋₆-haloalcoxi; R² es H, halógeno, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₁₋₆-alquilcarbonil-C₁₋₆-alquilo, C₁₋₆-alcoxicarbonil-C₁₋₆-alquilo, C₁₋₆-haloalquilcarbonil-C₁₋₆-alquilo, C₁₋₆-haloalcoxicarbonil-C₁₋₆-alquilo, C₁₋₆-alquilcarbonil-C₁₋₆-haloalquilo, C₁₋₆-alcoxicarbonil-C₁₋₆-haloalquilo, C₁₋₆-haloalquilcarbonil-C₁₋₆-haloalquilo, C₁₋₆-haloalcoxicarbonil-C₁₋₆-haloalquilo, OH, C₁₋₆-alcoxi, C₁₋₆-alcoxi-C₁₋₆-alcoxi, C₁₋₆-haloalcoxi-C₁₋₆-alcoxi, C₁₋₆-alcoxi-C₁₋₆-haloalcoxi, C₁₋₆-haloalcoxi-C₁₋₆-haloalcoxi, C₁₋₆-alcoxi-C₁₋₆-alcoxi-C₁₋₆-alcoxi, C₁₋₆-haloalcoxi, C₁₋₆-cianoalcoxi, C₁₋₆-hidroxialcoxi, C₃₋₆-alqueniloxi, C₃₋₆-alqueniloxi-C₁₋₆-alcoxi, C₃₋₆-haloalqueniloxi-C₁₋₆-haloalcoxi, C₃₋₆-alqueniloxi-C₁₋₆-haloalcoxi, C₃₋₆-haloalqueniloxi, C₃₋₆-alquiniloxi, C₃₋₆-haloalquiniloxi, C₃₋₆-alquiniloxi-C₁₋₆-alcoxi, C₃₋₆-haloalquiniloxi-C₁₋₆-haloalcoxi, C₃₋₆-alquiniloxi-C₁₋₆-haloalcoxi, C₃₋₆-alquiniloxi-C₃₋₆-alqueniloxi, C₃₋₆-haloalquiniloxi-C₃₋₆-alqueniloxi, C₃₋₆-alquiniloxi-C₃₋₆-haloalqueniloxi, C₃₋₆-haloalquiniloxi-C₃₋₆-haloalqueniloxi, C₃₋₆-alquiniloxi-C₃₋₆-alquiniloxi, C₃₋₆-haloalquiniloxi-C₃₋₆-alquiniloxi, C₃₋₆-alquiniloxi-C₃₋₆-haloalquiniloxi, C₃₋₆-haloalquiniloxi-C₃₋₆-haloalquiniloxi, (C₁₋₆-alquil)carbonil-C₁₋₆-alcoxi, (C₁₋₆-haloalquil)carbonil-C₁₋₆-haloalcoxi, -(C₁₋₆-haloalquil)carbonil-C₁₋₆-alcoxi, (C₁₋₆-alquil)carbonil-C₁₋₆-haloalcoxi, (C₁₋₆-alcoxi)carbonil-C₁₋₆-alcoxi, (C₁₋₆-haloalcoxi)carbonil-C₁₋₆-alcoxi, (C₁₋₆-alcoxi)carbonil-C₁₋₆-haloalcoxi, (C₁₋₆-haloalcoxi)carbonil-C₁₋₆-haloalcoxi, (C₁₋₆-alcoxi-C₁₋₆-alquil)carbonil-C₁₋₆-alcoxi, (C₁₋₆-haloalcoxi-C₁₋₆-alquil)carbonil-C₁₋₆-alcoxi, (C₁₋₆-alcoxi-C₁₋₆ haloalquil)carbonil-C₁₋₆-alcoxi, (C₁₋₆-alcoxi-C₁₋₆-alquil)carbonil-C₁₋₆-haloalcoxi, (C₁₋₆-haloalcoxi-C₁₋₆-haloalquil)carbonil-C₁₋₆-alcoxi, (C₁₋₆-haloalcoxi-C₁₋₆-alquil)carbonil-C₁₋₆-haloalcoxi, (C₁₋₆-alcoxi-C₁₋₆-haloalquil)carbonil-C₁₋₆-haloalcoxi, (C₁₋₆-haloalcoxi-C₁₋₆-haloalquil)carbonil-C₁₋₆-haloalcoxi, (C₁₋₆-alquiltio)carbonil-C₁₋₆-alcoxi, (C₁₋₆-haloalquiltio)carbonil-C₁₋₆-alcoxi, (C₁₋₆-alquiltio)carbonil-C₁₋₆-haloalcoxi, (C₁₋₆-haloalquiltio)carbonil-C₁₋₆-haloalcoxi, (C₁₋₆-alquiltio-C₁₋₆-alquil)carbonil-C₁₋₆-alcoxi, (C₁₋₆-haloalquiltio-C₁₋₆-alquil)carbonil-C₁₋₆-alcoxi, (C₁₋₆-alquiltio-C₁₋₆-haloalquil)carbonil-C₁₋₆-alcoxi, (C₁₋₆-alquiltio-C₁₋₆-alquil)carbonil-C₁₋₆-haloalcoxi, (C₁₋₆-haloalquiltio-C₁₋₆-haloalquil)carbonil-C₁₋₆-alcoxi, (C₁₋₆-haloalquiltio-C₁₋₆-alquil)carbonil-C₁₋₆-haloalcoxi, (C₁₋₆-alquiltio-C₁₋₆-haloalquil)carbonil-C₁₋₆-haloalcoxi, (C₁₋₆-haloalquiltio-C₁₋₆-haloalquil)carbonil-C₁₋₆-haloalcoxi, C₃₋₆-cicloalcoxi, C₃₋₆-halocicloalcoxi, (C₃₋₆-cicloalquil)C₁₋₆-alcoxi, (C₃₋₆-halocicloalquil)C₁₋₆-alcoxi, (C₃₋₆-cicloalquil)C₁₋₆-haloalcoxi, (C₃₋₆-halocicloalquil)C₁₋₆-haloalcoxi, aminocarbonil-C₁₋₆-alcoxi, aminocarbonil-C₁₋₆-haloalcoxi, N-(C₁₋₆-alquil)-aminocarbonil-C₁₋₆-alcoxi, N-(C₁₋₆-alquil)-aminocarbonil-C₁₋₆-haloalcoxi, N,N-di(C₁₋₆-alquil)-aminocarbonil-C₁₋₆-alcoxi, N,N-di(C₁₋₆-alquil)-aminocarbonil-C₁₋₆-haloalcoxi, O(di(fenil))C=N-O, (fenil)(C₁₋₆-alquil)C=N-O, [di(C₁₋₆-alquil)]C=N-O, (C₁₋₆-alquil)₃-silil-C₁₋₆-alcoxi, C₁₋₆-alquiltio, C₁₋₆-haloalquiltio, C₁₋₆-alcoxi-C₁₋₆-alquiltio, C₁₋₆-halo-alcoxi-C₁₋₆-alquiltio, C₁₋₆-alcoxi-C₁₋₆-haloalquiltio, C₁₋₆-haloalcoxi-C₁₋₆-haloalquiltio, C₁₋₆-alcoxi-C₁₋₆-alcoxi-C₁₋₆-alquiltio, C₁₋₆-cianoalquiltio, C₂₋₆-alqueniltio, C₂₋₆-haloalqueniltio, C₃₋₆-alqueniloxi-C₁₋₆-alquiltio, C₃₋₆-haloalqueniloxi-C₁₋₆-alquiltio, C₃₋₆-alqueniloxi-C₁₋₆-haloalquiltio, C₃₋₆-haloalqueniloxi-C₁₋₆-haloalquiltio, C₂₋₆-alquiniltio, C₂₋₆-haloalquiniltio, C₃₋₆-alquiniloxi-C₁₋₆-alquiltio, C₃₋₆-haloalquiniloxi-C₁₋₆-haloalquiltio, C₃₋₆-alquiniloxi-C₁₋₆-haloalquiltio, C₃₋₆-alquiniloxi-C₂₋₆-alqueniltio, C₃₋₆-haloalquiniloxi-C₂₋₆-alqueniltio, C₃₋₆-alquiniloxi-C₂₋₆-haloalqueniltio, C₃₋₆-haloalquiniloxi-C₂₋₆-haloalqueniltio, C₃₋₆-alquiniloxi-C₂₋₆-alquiniltio, C₃₋₆-haloalquiniloxi-C₂₋₆-alquiniltio, C₃₋₆-alquiniloxi-C₂₋₆-haloalquiniltio, C₃₋₆-haloalquiniloxi-C₂₋₆-haloalquiniltio, (C₁₋₆-alquil)carbonil-C₁₋₆-alquiltio, (C₁₋₆-haloalquil)carbonil-C₁₋₆-alquiltio, (C₁₋₆-alquil)carbonil-C₁₋₆-haloalquiltio, (C₁₋₆-haloalquil)carbonil-C₁₋₆-haloalquiltio, (C₁₋₆-alcoxi)carbonil-C₁₋₆-alquiltio, (C₁₋₆-haloalcoxi)carbonil-C₁₋₆-alquiltio, (C₁₋₆-alcoxi)carbonil-C₁₋₆-haloalquiltio (C₁₋₆-haloalcoxi)carbonil-C₁₋₆-haloalquiltio, (C₁₋₆-alcoxi-C₁₋₆-alquil)carbonil-C₁₋₆-alquiltio, (C₁₋₆-haloalcoxi-C₁₋₆-alquil)carbonil-C₁₋₆-alquiltio, (C₁₋₆-alcoxi-C₁₋₆-haloalquil)carbonil-C₁₋₆-alquiltio, (C₁₋₆-alcoxi-C₁₋₆-alquil)carbonil-C₁₋₆-haloalquiltio, (C₁₋₆-haloalcoxi-C₁₋₆-haloalquil)carbonil-C₁₋₆-alquiltio, (C₁₋₆-haloalcoxi-C₁₋₆-alquil)carbonil-C₁₋₆-haloalquiltio, (C₁₋₆-alcoxi-C₁₋₆-haloalquil)carbonil-C₁₋₆-haloalquiltio, (C₁₋₆-haloalcoxi-C₁₋₆-haloalquil)carbonil-C₁₋₆-haloalquiltio, (C₁₋₆-alquiltio)carbonil-C₁₋₆-alquiltio, (C₁₋₆ haloalquiltio)carbonil-C₁₋₆-alquiltio, (C₁₋₆-alquiltio)carbonil-C₁₋₆-haloalquiltio, (C₁₋₆-haloalquiltio)carbonil-C₁₋₆-haloalquiltio, (C₁₋₆-alquiltio-C₁₋₆-alquil)carbonil-C₁₋₆-alquiltio, (C₁₋₆-haloalquiltio-C₁₋₆-alquil)carbonil-C₁₋₆-alquiltio, (C₁₋₆-alquiltio-C₁₋₆-haloalquil)carbonil-C₁₋₆-alquiltio, (C₁₋₆-alquiltio-C₁₋₆-alquil)carbonil-C₁₋₆-haloalquiltio, (C₁₋₆-haloalquiltio-C₁₋₆-haloalquil)carbonil-C₁₋₆-alquiltio, (C₁₋₆-haloalquiltio-C₁₋₆-alquil)carbonil-C₁₋₆-haloalquiltio, (C₁₋₆-alquiltio-C₁₋₆-haloalquil)carbonil-C₁₋₆-haloalquiltio, (C₁₋₆-haloalquiltio-C₁₋₆-haloalquil)carbonil-C₁₋₆-haloalquiltio, C₃₋₆-cicloalquiltio, C₃₋₆-halocicloalquiltio, (C₃₋₆-cicloalquil)C₁₋₆-alquiltio, (C₃₋₆-cicloalquil)C₁₋₆-haloalquiltio, (C₃₋₆-halocicloalquil)C₁₋₆-alquiltio, (C₃₋₆-halocicloalquil)C₁₋₆-haloalquiltio, aminocarbonil-C₁₋₆-alquiltio, aminocarbonil-C₁₋₆-haloalquiltio, N-(C₁₋₆-alquil)-aminocarbonil-C₁₋₆-alquiltio, N-(C₁₋₆-haloalquil)-aminocarbonil-C₁₋₆-alquiltio, N-(C₁₋₆-alquil)-aminocarbonil-C₁₋₆-haloalquiltio, N-(C₁₋₆-haloalquil-aminocarbonil-C₁₋₆-haloalquiltio, N,N-di(C₁₋₆-alquil)-aminocarbonil-C₁₋₆-alquiltio, N,N-di(C₁₋₆-haloalquil)-aminocarbonil-C₁₋₆-alquiltio, N,N-di(C₁₋₆-alquil)-aminocarbonil-C₁₋₆-haloalquiltio, N,N-di(C₁₋₆-haloalquil)-aminocarbonil-C₁₋₆-haloalquiltio, NH₂, (C₁₋₆-alquil)amino, hidroxiamino, (C₁₋₆-alcoxi)amino, (C₃₋₆-cicloalcoxi)amino, (C₁₋₆-alquil)sulfinilamino, (C₁₋₆-alquil)sulfonilamino, (amino)sulfinilamino, [(C₁₋₆-alquil)amino]sulfinilamino, (amino)sulfonilamino, [(C₁₋₆-alquil)amino]sulfonilamino, [di(C₁₋₆-alquil)amino]sulfonilamino, di(C₁₋₆-alquil)amino, (hidroxi)(C₁₋₆-alquil)amino, (hidroxi)(C₁₋₆-cicloalquil)amino, (C₁₋₆-alcoxi)(C₁₋₆-alquil)amino, (C₁₋₆-alcoxi)(C₃₋₆-cicloalquil)amino, (C₃₋₆-cicloalcoxi)(C₁₋₆-alquil)amino, (C₃₋₆-cicloalcoxi)-(C₃₋₆-cicloalquil)amino, [(C₁₋₆-alquil)sulfinil](C₁₋₆-alquil)amino, [(C₁₋₆-alquil)sulfonil](C₁₋₆-alquil)amino, [di(C₁₋₆-alquil)amino]sulfinilamino, [di(C₁₋₆-alquil)amino]sulfonilamino, feniloxi, fenil-C₁₋₆-alcoxi, feniltio, fenil-C₁₋₆-alquiltio, fenilamino, (C₁₋₆-alquil)(fenil)amino, (heteroaril)oxi, heteroaril-C₁₋₆-alcoxi, (heterociclil)oxi, heterociclil-C₁₋₆-alcoxi, en donde los sustituyentes de fenilo, heteroarilo y heterociclilo, independientemente entre sí, son no sustituidos o sustituidos con 1 a 5 sustituyentes seleccionados del grupo que consiste en halógeno, CN, NO₂, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₁₋₆-alcoxi o C₁₋₆-haloalcoxi; R³ es halógeno, CN, NO₂, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₁₋₆-alquilcarbonilo, C₂₋₆-alquenilo, C₂₋₆-haloalquenilo, C₂₋₆-alquinilo, C₂₋₆-haloalquinilo, C₁₋₆-alcoxi, C₁₋₆-haloalcoxi, C₃₋₆-alqueniloxi, C₃₋₆-haloalqueniloxi, C₃₋₆-alquiniloxi, C₃₋₆-haloalquiniloxi, C₁₋₆-alcoxi-C₁₋₆-alcoxi, hidroxicarbonilo, C₁₋₆-alcoxicarbonilo, C₁₋₆-alquiltio, C₁₋₆-haloalquiltio, NH₂, (C₁₋₆-alquil)amino, di(C₁₋₆-alquil)amino, (C₁₋₆-alquil)sulfinilo, (C₁₋₆-alquil)sulfonilo, C₃₋₆-cicloalquilo, (C₃₋₆-cicloalquil)oxi o fenilo; en donde los sustituyentes de cicloalquilo, (cicloalquil)oxi o fenilo, independientemente entre sí, son no sustituidos o sustituidos con 1 a 5 sustituyentes, seleccionados del grupo que consiste en halógeno, CN, NO₂, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₁₋₆-alcoxi o C₁₋₆-haloalcoxi; y R⁴ R⁵, R⁶ y R⁷ son, independientemente entre sí, H, halógeno, CN, NO₂, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₁₋₆-alquilcarbonilo, C₂₋₆-alquenilo, C₂₋₆-haloalquenilo, C₂₋₆-alquinilo, C₂₋₆-haloalquinilo, C₁₋₆-alcoxi, C₁₋₆-haloalcoxi, C₃₋₆-alqueniloxi, C₃₋₆-haloalqueniloxi, C₃₋₆-alquiniloxi, C₃₋₆-haloalquiniloxi, C₁₋₆-alcoxi-C₁₋₆-alcoxi, hidroxicarbonilo, C₁₋₆-alcoxicarbonilo, C₁₋₆-alquiltio, C₁₋₆-haloalquiltio, NH₂, (C₁₋₆-alquil)amino, di(C₁₋₆-alquil)amino, (C₁₋₆-alquil)sulfinilo, (C₁₋₆-alquil)sulfonilo, C₃₋₆-cicloalquilo, (C₃₋₆-cicloalquil)oxi o fenilo; en donde los sustituyentes de cicloalquilo, (cicloalquil)oxi o fenilo, independientemente entre sí, son no sustituidos o sustituidos con 1 a 5 sustituyentes seleccionados del grupo que consiste en halógeno, CN, NO₂, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₁₋₆-alcoxi o C₁₋₆-haloalcoxi; que incluyen derivados o sales aceptables en la agricultura de los compuestos de la fórmula (1) que tienen un grupo carboxilo; y al menos un compuesto activo adicional seleccionado de: B) herbicidas de las clases b1) a b15): b1) inhibidores de la biosíntesis de lípidos; b2) inhibidores de acetolactato sintasa (inhibidores de ALS); b3) inhibidores de la fotosíntesis; b4) inhibidores de protoporfirinógeno-IX oxidasa, b5) herbicidas blanqueadores; b6) inhibidores de enolpiruvil shiquimato 3-fosfato sintasa (inhibidores de EPSP); b7) inhibidores de glutamina sintetasa; b8) inhibidores de 7,8-dihidropteroato sintasa (inhibidores de DHP); b9) inhibidores de mitosis; b10) inhibidores de la síntesis de ácidos grasos de cadena muy larga (inhibidores de VLCFA); b11) inhibidores de la biosíntesis de celulosa; b12) herbicidas desacopladores; b13) herbicidas auxínicos; b14) inhibidores del transporte de auxina; y b15) otros herbicidas seleccionados del grupo que consiste en bromobutide, chlorflurenol, chlorflurenol-metilo, cinmethylin, cumyluron, dalapon, dazomet, difenzoquat, difenzoquat-metilsulfato, dimethipin, DSMA, dymron, endothal y sus sales, etobenzanid, flamprop, flamprop-isopropilo, flamprop-metilo, flamprop-M-isopropilo, flamprop-M-metilo, flurenol, flurenol-butilo, flurprimidol, fosamine, fosamine-amonio, findanofan, indaziflam, hidrazida maleica, mefluidide, metam, methiozolin, azida de metilo, bromuro de metilo, metil-dymron, yoduro de metilo; MSMA, ácido oleico, oxaziclomefone, ácido pelargónico, pyributicarb, quinoclamine, triaziflam, tridiphane y 6-cloro-3-(2-ciclopropil-6-metilfenoxi)-4-piridazinol, y sus sales y ésteres; lo que incluye sus sales o derivados aceptables en la agricultura. Reivindicación 6: La composición de acuerdo con cualquiera de las reivindicaciones anteriores, caracterizada porque en el compuesto de la fórmula (1), R¹ es C₃₋₆-cicloalquilo; R² es OH o C₁₋₆-alcoxi; R³ es halógeno; R⁴, R⁶ y R⁷ son H; R⁵ es H o halógeno. Reivindicación 7: La composición de acuerdo con cualquiera de las reivindicaciones anteriores, caracterizada porque en el compuesto de la fórmula (1), R¹ es c-C₃H₅; R² es OH u OCH₃; R³ es Cl; R⁴, R⁶ y R⁷ son H; R⁵ es H o F. Reivindicación 14: Un método para controlar vegetación no deseada, caracterizado porque comprende permitir que una composición herbicida de acuerdo con cualquiera de las reivindicaciones anteriores actúe en plantas, en su entorno o en las semillas.
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| Application Number | Priority Date | Filing Date | Title |
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| EP16180303 | 2016-07-20 |
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| ARP170102021A AR109100A1 (es) | 2016-07-20 | 2017-07-19 | Composiciones herbicidas que comprenden fenilpirimidinas |
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| US (1) | US10966426B2 (es) |
| EP (1) | EP3487300B1 (es) |
| CN (1) | CN109475123B (es) |
| AR (1) | AR109100A1 (es) |
| AU (1) | AU2017298874A1 (es) |
| BR (1) | BR112018076700A2 (es) |
| CA (1) | CA3029873A1 (es) |
| EA (1) | EA201990279A1 (es) |
| WO (1) | WO2018015180A1 (es) |
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| US11180470B2 (en) | 2016-07-25 | 2021-11-23 | Basf Se | Herbicidal pyrimidine compounds |
| WO2018019555A1 (en) | 2016-07-26 | 2018-02-01 | Basf Se | Herbicidal pyrimidine compounds |
| US10863743B2 (en) | 2016-07-29 | 2020-12-15 | Basf Se | Method for controlling PPO resistant weeds |
| EP3555053B1 (en) | 2016-12-16 | 2021-02-17 | Basf Se | Herbicidal phenyltriazolinones |
| WO2019006358A1 (en) * | 2017-06-30 | 2019-01-03 | Syngenta Participations Ag | HERBICIDE COMPOSITION AND METHOD OF USE |
| BR112020008084B1 (pt) | 2017-11-23 | 2023-11-14 | Basf Se | Fenil éteres, composição herbicida, processo de preparação de composições ativas, método de controle de vegetação indesejada e uso dos fenil éteres |
| CA3080276A1 (en) | 2017-11-23 | 2019-05-31 | Basf Se | Herbicidal pyridylethers |
| CA3080449A1 (en) | 2017-11-27 | 2019-05-31 | Basf Se | Crystalline forms of ethyl 2-[[3-[[3-chloro-5-fluoro-6-[3-methyl-2,6-dioxo-4-(trifluoromethyl)pyrimidin-1-yl]-2-pyridyl]oxy]-2-pyridyl]oxy]acetate |
| US11390589B2 (en) * | 2018-06-04 | 2022-07-19 | Bayer Aktiengesellschaft | Herbicidally active substituted phenylpyrimidines |
| AU2020220608A1 (en) * | 2019-02-15 | 2021-08-19 | Syngenta Crop Protection Ag | Herbicidal compositions |
| CA3128409A1 (en) * | 2019-02-15 | 2020-08-20 | Syngenta Crop Protection Ag | Herbicidal compositions |
| MX2022015189A (es) * | 2020-06-02 | 2023-01-04 | Bayer Ag | Herbicidas selectivos en base a carboxamidas de isoxazolina sustituidas y metcamifen. |
| AU2022276592A1 (en) * | 2021-05-21 | 2024-01-18 | Rallis India Limited | Herbicide composition and process for preparing thereof |
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| EP0136976A3 (de) * | 1983-08-23 | 1985-05-15 | Ciba-Geigy Ag | Verwendung von Phenylpyrimidinen als Pflanzenregulatoren |
| BR8600161A (pt) | 1985-01-18 | 1986-09-23 | Plant Genetic Systems Nv | Gene quimerico,vetores de plasmidio hibrido,intermediario,processo para controlar insetos em agricultura ou horticultura,composicao inseticida,processo para transformar celulas de plantas para expressar uma toxina de polipeptideo produzida por bacillus thuringiensis,planta,semente de planta,cultura de celulas e plasmidio |
| NZ231804A (en) | 1988-12-19 | 1993-03-26 | Ciba Geigy Ag | Insecticidal toxin from leiurus quinquestriatus hebraeus |
| EP0392225B1 (en) | 1989-03-24 | 2003-05-28 | Syngenta Participations AG | Disease-resistant transgenic plants |
| DE69018772T2 (de) | 1989-11-07 | 1996-03-14 | Pioneer Hi Bred Int | Larven abtötende Lektine und darauf beruhende Pflanzenresistenz gegen Insekten. |
| UA48104C2 (uk) | 1991-10-04 | 2002-08-15 | Новартіс Аг | Фрагмент днк, який містить послідовність,що кодує інсектицидний протеїн, оптимізовану для кукурудзи,фрагмент днк, який забезпечує направлену бажану для серцевини стебла експресію зв'язаного з нею структурного гена в рослині, фрагмент днк, який забезпечує специфічну для пилку експресію зв`язаного з нею структурного гена в рослині, рекомбінантна молекула днк, спосіб одержання оптимізованої для кукурудзи кодуючої послідовності інсектицидного протеїну, спосіб захисту рослин кукурудзи щонайменше від однієї комахи-шкідника |
| US5530195A (en) | 1994-06-10 | 1996-06-25 | Ciba-Geigy Corporation | Bacillus thuringiensis gene encoding a toxin active against insects |
| BR9610155A (pt) * | 1995-08-10 | 1999-01-05 | Sumitomo Chemical Co | Derivados de pirimidin-4-ona seu uso intermediários para a sua produção e processos para a produção desses intermediários |
| JO2308B1 (en) | 1999-05-31 | 2005-09-12 | اف. هوفمان- لاروش أيه جي | Derivatives of phenylpyrmidine |
| WO2002015701A2 (en) | 2000-08-25 | 2002-02-28 | Syngenta Participations Ag | Bacillus thuringiensis crystal protein hybrids |
| US7230167B2 (en) | 2001-08-31 | 2007-06-12 | Syngenta Participations Ag | Modified Cry3A toxins and nucleic acid sequences coding therefor |
| WO2003052073A2 (en) | 2001-12-17 | 2003-06-26 | Syngenta Participations Ag | Novel corn event |
| NZ553172A (en) | 2004-09-03 | 2009-07-31 | Syngenta Ltd | Isoxazoline derivatives and their use as herbicides |
| PL1799657T3 (pl) | 2004-10-05 | 2010-05-31 | Syngenta Ltd | Pochodne izoksazoliny i ich zastosowanie jako herbicydów |
| GB0526044D0 (en) | 2005-12-21 | 2006-02-01 | Syngenta Ltd | Novel herbicides |
| GB0603891D0 (en) | 2006-02-27 | 2006-04-05 | Syngenta Ltd | Novel herbicides |
| BR112017016273A2 (pt) | 2015-01-29 | 2018-03-27 | Basf Se | fenilpiridinas de fórmula, processo para a preparação de fenilpiridinas, cloretos de ácido, composição herbicida, processo para a preparação de composições, método para o controle da vegetação e utilização |
| EP3250034B1 (en) | 2015-01-30 | 2020-03-11 | Basf Se | Herbicidal phenylpyrimidines |
| CN109561685A (zh) | 2016-07-25 | 2019-04-02 | 巴斯夫欧洲公司 | 除草的嘧啶化合物 |
| US11180470B2 (en) | 2016-07-25 | 2021-11-23 | Basf Se | Herbicidal pyrimidine compounds |
| WO2018019555A1 (en) | 2016-07-26 | 2018-02-01 | Basf Se | Herbicidal pyrimidine compounds |
| WO2018019765A1 (en) | 2016-07-27 | 2018-02-01 | Basf Se | Herbicidal pyrimidine compounds |
| CA3032014A1 (en) | 2016-07-27 | 2018-02-01 | BASF Agro B.V. | Plants having increased tolerance to herbicides |
| WO2018019574A1 (en) | 2016-07-28 | 2018-02-01 | Basf Se | Herbicidal pyrimidine compounds |
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2017
- 2017-07-07 CA CA3029873A patent/CA3029873A1/en not_active Abandoned
- 2017-07-07 EA EA201990279A patent/EA201990279A1/ru unknown
- 2017-07-07 EP EP17737259.6A patent/EP3487300B1/en active Active
- 2017-07-07 US US16/318,969 patent/US10966426B2/en not_active Expired - Fee Related
- 2017-07-07 WO PCT/EP2017/067065 patent/WO2018015180A1/en not_active Ceased
- 2017-07-07 CN CN201780044734.1A patent/CN109475123B/zh not_active Expired - Fee Related
- 2017-07-07 AU AU2017298874A patent/AU2017298874A1/en not_active Abandoned
- 2017-07-07 BR BR112018076700A patent/BR112018076700A2/pt not_active IP Right Cessation
- 2017-07-19 AR ARP170102021A patent/AR109100A1/es unknown
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| AU2017298874A1 (en) | 2019-01-03 |
| CN109475123A (zh) | 2019-03-15 |
| US20190297886A1 (en) | 2019-10-03 |
| WO2018015180A1 (en) | 2018-01-25 |
| BR112018076700A2 (pt) | 2019-04-02 |
| EA201990279A1 (ru) | 2019-08-30 |
| CA3029873A1 (en) | 2018-01-25 |
| EP3487300A1 (en) | 2019-05-29 |
| EP3487300B1 (en) | 2021-04-07 |
| CN109475123B (zh) | 2021-07-09 |
| US10966426B2 (en) | 2021-04-06 |
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