AR077926A1 - ACTIVE HERBICIDE COMPOSITION INCLUDING BENZOXAZINONAS - Google Patents
ACTIVE HERBICIDE COMPOSITION INCLUDING BENZOXAZINONASInfo
- Publication number
- AR077926A1 AR077926A1 ARP100103002A AR077926A1 AR 077926 A1 AR077926 A1 AR 077926A1 AR P100103002 A ARP100103002 A AR P100103002A AR 077926 A1 AR077926 A1 AR 077926A1
- Authority
- AR
- Argentina
- Prior art keywords
- inhibitors
- methyl
- herbicides
- alkyl
- hydrogen
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title abstract 6
- 239000000203 mixture Substances 0.000 title abstract 4
- 230000002363 herbicidal effect Effects 0.000 title abstract 2
- 239000003112 inhibitor Substances 0.000 abstract 15
- -1 benzoxazinone compound Chemical class 0.000 abstract 6
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 3
- YNQSILKYZQZHFJ-UHFFFAOYSA-N R-29148 Chemical compound CC1CN(C(=O)C(Cl)Cl)C(C)(C)O1 YNQSILKYZQZHFJ-UHFFFAOYSA-N 0.000 abstract 3
- 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 abstract 2
- 229930192334 Auxin Natural products 0.000 abstract 2
- 239000002363 auxin Substances 0.000 abstract 2
- 230000015572 biosynthetic process Effects 0.000 abstract 2
- GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 abstract 2
- 150000002431 hydrogen Chemical group 0.000 abstract 2
- SEOVTRFCIGRIMH-UHFFFAOYSA-N indole-3-acetic acid Chemical compound C1=CC=C2C(CC(=O)O)=CNC2=C1 SEOVTRFCIGRIMH-UHFFFAOYSA-N 0.000 abstract 2
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 150000004669 very long chain fatty acids Chemical class 0.000 abstract 2
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- 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 abstract 1
- 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 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
- 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
- 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
- PFJJMJDEVDLPNE-UHFFFAOYSA-N Benoxacor Chemical compound C1=CC=C2N(C(=O)C(Cl)Cl)C(C)COC2=C1 PFJJMJDEVDLPNE-UHFFFAOYSA-N 0.000 abstract 1
- 239000005644 Dazomet Substances 0.000 abstract 1
- YRMLFORXOOIJDR-UHFFFAOYSA-N Dichlormid Chemical compound ClC(Cl)C(=O)N(CC=C)CC=C YRMLFORXOOIJDR-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
- NRFQZTCQAYEXEE-UHFFFAOYSA-N Fenclorim Chemical compound ClC1=CC(Cl)=NC(C=2C=CC=CC=2)=N1 NRFQZTCQAYEXEE-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
- UKSLKNUCVPZQCQ-UHFFFAOYSA-N Fluxofenim Chemical compound C=1C=C(Cl)C=CC=1C(C(F)(F)F)=NOCC1OCCO1 UKSLKNUCVPZQCQ-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-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
- 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
- GRSMWKLPSNHDHA-UHFFFAOYSA-N Naphthalic anhydride Chemical compound C1=CC(C(=O)OC2=O)=C3C2=CC=CC3=C1 GRSMWKLPSNHDHA-UHFFFAOYSA-N 0.000 abstract 1
- FCOHEOSCARXMMS-UHFFFAOYSA-N Oxaziclomefone Chemical compound C1OC(C)=C(C=2C=CC=CC=2)C(=O)N1C(C)(C)C1=CC(Cl)=CC(Cl)=C1 FCOHEOSCARXMMS-UHFFFAOYSA-N 0.000 abstract 1
- 102000004316 Oxidoreductases Human genes 0.000 abstract 1
- 108090000854 Oxidoreductases Proteins 0.000 abstract 1
- 239000005643 Pelargonic acid Substances 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
- 239000002253 acid Substances 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical group [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 abstract 1
- 208000014347 autosomal dominant hyaline body myopathy Diseases 0.000 abstract 1
- OTSAMNSACVKIOJ-UHFFFAOYSA-N azane;carbamoyl(ethoxy)phosphinic acid Chemical compound [NH4+].CCOP([O-])(=O)C(N)=O OTSAMNSACVKIOJ-UHFFFAOYSA-N 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
- 230000008166 cellulose biosynthesis Effects 0.000 abstract 1
- ICJSJAJWTWPSBD-UHFFFAOYSA-N cloquintocet Chemical compound C1=CN=C2C(OCC(=O)O)=CC=C(Cl)C2=C1 ICJSJAJWTWPSBD-UHFFFAOYSA-N 0.000 abstract 1
- 150000001875 compounds Chemical class 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
- 102000005396 glutamine synthetase Human genes 0.000 abstract 1
- 108020002326 glutamine synthetase Proteins 0.000 abstract 1
- 229910052736 halogen Chemical group 0.000 abstract 1
- 150000002367 halogens Chemical group 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 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
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 abstract 1
- 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 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
- 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
- PBTHJVDBCFJQGG-UHFFFAOYSA-N methyl azide Chemical compound CN=[N+]=[N-] PBTHJVDBCFJQGG-UHFFFAOYSA-N 0.000 abstract 1
- 229940102396 methyl bromide Drugs 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
- 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
- QYOJSKGCWNAKGW-HCWXCVPCSA-N shikimate-3-phosphate Chemical compound O[C@H]1CC(C(O)=O)=C[C@H](OP(O)(O)=O)[C@@H]1O QYOJSKGCWNAKGW-HCWXCVPCSA-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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
-
- 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/84—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,4
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Reivindicacion 1: Una composicion herbicida caracterizada porque comprende: A) por lo menos un compuesto de benzoxazinona de la formula (1), donde R1 es hidrogeno o C1-6-alquilo; R2 es hidrogeno, NH2, C1-6-alquilo o C3-6-alquinilo; R3 es hidrogeno o halogeno; R4 es hidrogeno, C1-6-alquilo, C1-6-haloalquilo, C3-6-cicloalquilo, C3-6-alquenilo, C3-6-haloalquenilo, C3-6-alquinilo, C3-6-haloalquinilo, C1-6-alcoxi o C3-6-cicloalquil-C1-6-alquilo; X es O o S; Y es O o S; y por lo menos un compuesto activo adicional seleccionado de entre B) herbicidas de las clases b1) a b15): b1) inhibidores de la biosíntesis lípida; b2) inhibidores de acetolacto sintasa (inhibidores ALS); b3) inhibidores de la fotosíntesis; b4) inhibidores de protoporfirinogeno-lX oxidasa, b5) herbicidas blanqueadores; b6) inhibidores de enolpiruvilo shikimato 3-fosfato sintasa (inhibidores EPSP); b7) inhibidores de glutamina sintetasa; b8) inhibidores de 7,8-dihidropteroato sintasa (inhibidores DHP); b9) inhibidores de mitosa; b10) inhibidores de la síntesis de ácidos grasos de cadena muy larga (inhibidores VLCFA); b11) inhibidores de la biosíntesis de celulosa; b12) herbicidas desacopladores; b13) herbicidas de auxina; b14) inhibidores del transporte de auxina; y b15) otros herbicidas seleccionados del grupos que abarca bromobutida, clorflurenol, clorflurenol-metilo, cinmetilina, cumilurona, dalapona, dazomet, difenozoquat, difenozoquat-metilosulfato, dimetipina, DSMA, dimrona, endotal y sus sales, etobenzanid, flamprop, flamprop-isopropilo, flamprop-metilo, flamprop-M-isopropilo, flamprop-M-metilo, flurenol, flurenol-butilo, flurprimidol, fosamina, fosamina-amonio, indanofano, indaziflam, hidrazida maleica, mefluidida, metam, metil azida, metil bromuro, metil-dimrona, metil yoduro, MSMA, ácido olico, oxaziclomefona, ácido pelargonico, piributicarb, quinoclamina, triaziflam, tridifano y 6-cloro-3-(2-ciclopropil-6-metilofenoxi)-4-piridazinaol (CAS 499223-49-3) y sus sales y ésteres; y C) aseguradores. Reivindicacion 5: Una composicion de acuerdo con cualquiera de las reivindicaciones 1 a 4, caracterizada porque comprende por lo menos un asegurador seleccionado del grupo que abarca benoxacor, cloquintocet, cyometrinilo, ciprosulfamida, diclormid, diciclonon, dietolato, fenclorazol, fenclorim, flurazol, fluxofenim, furilazol, isoxadifeno, mefenpir, mefenato, anhídrido naftálico, oxabetrinilo, 4-(dicloroacetil)-1-oxa-4-azaspiro[4.5]decano (MON4660, CAS 71526-07-3) y 2,2,5-trimetil-3-(dicloroacetil)-1,3-oxazolidina (R-29148, CAS 52836-31-4). Reivindicacion 12: El uso de composiciones de acuerdo con cualquiera de las reivindicaciones 1 a 8, caracterizada por controlar vegetacion indeseada.Claim 1: A herbicidal composition characterized in that it comprises: A) at least one benzoxazinone compound of the formula (1), wherein R 1 is hydrogen or C 1-6 alkyl; R2 is hydrogen, NH2, C1-6-alkyl or C3-6-alkynyl; R3 is hydrogen or halogen; R4 is hydrogen, C1-6-alkyl, C1-6-haloalkyl, C3-6-cycloalkyl, C3-6-alkenyl, C3-6-haloalkenyl, C3-6-alkynyl, C3-6-haloalkynyl, C1-6- alkoxy or C3-6-cycloalkyl-C1-6-alkyl; X is O or S; Y is O or S; and at least one additional active compound selected from B) herbicides of classes b1) to b15): b1) lipid biosynthesis inhibitors; b2) acetolacto synthase inhibitors (ALS inhibitors); b3) photosynthesis inhibitors; b4) protoporphyrinogen-lX oxidase inhibitors, b5) bleaching herbicides; b6) enolpiruvilo shikimate 3-phosphate synthase inhibitors (EPSP inhibitors); b7) glutamine synthetase inhibitors; b8) 7,8-dihydropteroate synthase inhibitors (DHP inhibitors); b9) mitosa inhibitors; b10) inhibitors of the synthesis of very long chain fatty acids (VLCFA inhibitors); b11) cellulose biosynthesis inhibitors; b12) decoupling herbicides; b13) auxin herbicides; b14) auxin transport inhibitors; and b15) other herbicides selected from the groups encompassing bromobutide, chlorflurenol, chlorflurenol-methyl, cinmethyline, cumilurone, dalapona, dazomet, diphenozoquat, diphenozoquat-methylosulfate, dimethipine, DSMA, dimrona, endotal and its salts, etobenzanid, flamproprop, flamproprop-flampropyl-flampropyl , flamprop-methyl, flamprop-M-isopropyl, flamprop-M-methyl, flurenol, flurenol-butyl, flurprimidol, fosamine, phosamine-ammonium, indanophane, indaziflam, maleic hydrazide, mefluidide, metam, methyl azide, methyl bromide, methyl- dimrona, methyl iodide, MSMA, olic acid, oxaziclomefone, pelargonic acid, pyributicarb, quinoclamine, triaziflam, tridiphane and 6-chloro-3- (2-cyclopropyl-6-methylphenoxy) -4-pyridazinaol (CAS 499223-49-3) and its salts and esters; and C) insurers. Claim 5: A composition according to any one of claims 1 to 4, characterized in that it comprises at least one insurer selected from the group comprising benoxacor, cloquintocet, cyometrinyl, ciprosulfamide, dichlormid, diciclonon, dietolato, fenclorazol, fenclorim, flurazol, fluxofenim , furilazole, isoxadifen, mefenpyr, methanate, naphthalic anhydride, oxabetrinyl, 4- (dichloroacetyl) -1-oxa-4-azaspiro [4.5] decane (MON4660, CAS 71526-07-3) and 2,2,5-trimethyl- 3- (dichloroacetyl) -1,3-oxazolidine (R-29148, CAS 52836-31-4). Claim 12: The use of compositions according to any of claims 1 to 8, characterized by controlling unwanted vegetation.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP09167917 | 2009-08-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR077926A1 true AR077926A1 (en) | 2011-10-05 |
Family
ID=43503082
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP100103002 AR077926A1 (en) | 2009-08-14 | 2010-08-13 | ACTIVE HERBICIDE COMPOSITION INCLUDING BENZOXAZINONAS |
Country Status (4)
| Country | Link |
|---|---|
| AR (1) | AR077926A1 (en) |
| TW (1) | TW201109321A (en) |
| UY (1) | UY32838A (en) |
| WO (1) | WO2011018486A2 (en) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2443102B1 (en) | 2009-06-19 | 2013-04-17 | Basf Se | Herbicidal benzoxazinones |
| CN103221409B (en) | 2010-10-01 | 2016-03-09 | 巴斯夫欧洲公司 | Herbicidal benzoxazinones |
| EP2651226B1 (en) * | 2010-12-15 | 2016-11-23 | Basf Se | Herbicidal compositions |
| DE112011104396T5 (en) | 2010-12-16 | 2013-10-10 | Basf Se | Plants with increased tolerance to herbicides |
| CN102365965B (en) * | 2011-11-04 | 2014-06-18 | 陕西美邦农药有限公司 | Pesticide composition containing ethoxysulfuron |
| CN102334496B (en) * | 2011-11-09 | 2013-08-14 | 山东胜邦绿野化学有限公司 | Composite herbicide and preparation method thereof |
| CN102342281A (en) * | 2011-11-18 | 2012-02-08 | 江苏龙灯化学有限公司 | Weeding composition |
| UY34653A (en) * | 2012-03-05 | 2013-10-31 | Syngenta Participations Ag | ? HERBICIDE COMPOSITIONS THAT PROVIDE EXTENSIVE WEED CONTROL WITH REDUCED RESULTING PHYTO TOXICITY FOR CULTIVARS ?. |
| AR091489A1 (en) * | 2012-06-19 | 2015-02-11 | Basf Se | PLANTS THAT HAVE A GREATER TOLERANCE TO HERBICIDES INHIBITORS OF PROTOPORFIRINOGENO OXIDASA (PPO) |
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- 2010-08-12 WO PCT/EP2010/061718 patent/WO2011018486A2/en not_active Ceased
- 2010-08-12 UY UY32838A patent/UY32838A/en unknown
- 2010-08-13 AR ARP100103002 patent/AR077926A1/en unknown
- 2010-08-13 TW TW99127178A patent/TW201109321A/en unknown
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| TW201109321A (en) | 2011-03-16 |
| WO2011018486A2 (en) | 2011-02-17 |
| UY32838A (en) | 2011-01-31 |
| WO2011018486A3 (en) | 2011-10-13 |
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