ECSP11010821A - Combination of herbicides with difluoromethanesulfonilanilides substituted with dimethoxytriazinyl - Google Patents
Combination of herbicides with difluoromethanesulfonilanilides substituted with dimethoxytriazinylInfo
- Publication number
- ECSP11010821A ECSP11010821A ECSP11010821A ECSP11010821A EC SP11010821 A ECSP11010821 A EC SP11010821A EC SP11010821 A ECSP11010821 A EC SP11010821A EC SP11010821 A ECSP11010821 A EC SP11010821A
- Authority
- EC
- Ecuador
- Prior art keywords
- herbicides
- taken
- combination
- methyl
- difluoromethanesulfonilanilides
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title abstract 3
- -1 dimethoxytriazinyl Chemical group 0.000 title 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- YNWVFADWVLCOPU-MDWZMJQESA-N (1E)-1-(4-chlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pent-1-en-3-ol Chemical compound C1=NC=NN1/C(C(O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1 YNWVFADWVLCOPU-MDWZMJQESA-N 0.000 abstract 1
- RMOGWMIKYWRTKW-UONOGXRCSA-N (S,S)-paclobutrazol Chemical compound C([C@@H]([C@@H](O)C(C)(C)C)N1N=CN=C1)C1=CC=C(Cl)C=C1 RMOGWMIKYWRTKW-UONOGXRCSA-N 0.000 abstract 1
- XUHGTGGPZFJRMF-UHFFFAOYSA-N 1,3-dihydropyrazole-2-carboxylic acid Chemical compound OC(=O)N1CC=CN1 XUHGTGGPZFJRMF-UHFFFAOYSA-N 0.000 abstract 1
- DHYXNIKICPUXJI-UHFFFAOYSA-N 1-(2,4-dichlorophenyl)-n-(2,4-difluorophenyl)-5-oxo-n-propan-2-yl-1,2,4-triazole-4-carboxamide Chemical compound C=1C=C(F)C=C(F)C=1N(C(C)C)C(=O)N(C1=O)C=NN1C1=CC=C(Cl)C=C1Cl DHYXNIKICPUXJI-UHFFFAOYSA-N 0.000 abstract 1
- NUPJIGQFXCQJBK-UHFFFAOYSA-N 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)-5-(methoxymethyl)nicotinic acid Chemical compound OC(=O)C1=CC(COC)=CN=C1C1=NC(C)(C(C)C)C(=O)N1 NUPJIGQFXCQJBK-UHFFFAOYSA-N 0.000 abstract 1
- CLQMBPJKHLGMQK-UHFFFAOYSA-N 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)nicotinic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC=CC=C1C(O)=O CLQMBPJKHLGMQK-UHFFFAOYSA-N 0.000 abstract 1
- CABMTIJINOIHOD-UHFFFAOYSA-N 2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]quinoline-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC2=CC=CC=C2C=C1C(O)=O CABMTIJINOIHOD-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 1
- CASLETQIYIQFTQ-UHFFFAOYSA-N 3-[[5-(difluoromethoxy)-1-methyl-3-(trifluoromethyl)pyrazol-4-yl]methylsulfonyl]-5,5-dimethyl-4h-1,2-oxazole Chemical compound CN1N=C(C(F)(F)F)C(CS(=O)(=O)C=2CC(C)(C)ON=2)=C1OC(F)F CASLETQIYIQFTQ-UHFFFAOYSA-N 0.000 abstract 1
- PVSGXWMWNRGTKE-UHFFFAOYSA-N 5-methyl-2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]pyridine-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC=C(C)C=C1C(O)=O PVSGXWMWNRGTKE-UHFFFAOYSA-N 0.000 abstract 1
- DVOODWOZJVJKQR-UHFFFAOYSA-N 5-tert-butyl-3-(2,4-dichloro-5-prop-2-ynoxyphenyl)-1,3,4-oxadiazol-2-one Chemical group O=C1OC(C(C)(C)C)=NN1C1=CC(OCC#C)=C(Cl)C=C1Cl DVOODWOZJVJKQR-UHFFFAOYSA-N 0.000 abstract 1
- KLSJWNVTNUYHDU-UHFFFAOYSA-N Amitrole Chemical compound NC1=NC=NN1 KLSJWNVTNUYHDU-UHFFFAOYSA-N 0.000 abstract 1
- JDWQITFHZOBBFE-UHFFFAOYSA-N Benzofenap Chemical compound C=1C=C(Cl)C(C)=C(Cl)C=1C(=O)C=1C(C)=NN(C)C=1OCC(=O)C1=CC=C(C)C=C1 JDWQITFHZOBBFE-UHFFFAOYSA-N 0.000 abstract 1
- LLQPHQFNMLZJMP-UHFFFAOYSA-N Fentrazamide Chemical compound N1=NN(C=2C(=CC=CC=2)Cl)C(=O)N1C(=O)N(CC)C1CCCCC1 LLQPHQFNMLZJMP-UHFFFAOYSA-N 0.000 abstract 1
- 239000005566 Imazamox Substances 0.000 abstract 1
- 239000005981 Imazaquin Substances 0.000 abstract 1
- JLLJHQLUZAKJFH-UHFFFAOYSA-N Isouron Chemical compound CN(C)C(=O)NC=1C=C(C(C)(C)C)ON=1 JLLJHQLUZAKJFH-UHFFFAOYSA-N 0.000 abstract 1
- 239000005570 Isoxaben Substances 0.000 abstract 1
- LRUUNMYPIBZBQH-UHFFFAOYSA-N Methazole Chemical compound O=C1N(C)C(=O)ON1C1=CC=C(Cl)C(Cl)=C1 LRUUNMYPIBZBQH-UHFFFAOYSA-N 0.000 abstract 1
- CHNUNORXWHYHNE-UHFFFAOYSA-N Oxadiazon Chemical compound C1=C(Cl)C(OC(C)C)=CC(N2C(OC(=N2)C(C)(C)C)=O)=C1Cl CHNUNORXWHYHNE-UHFFFAOYSA-N 0.000 abstract 1
- 239000005985 Paclobutrazol Substances 0.000 abstract 1
- ORFPWVRKFLOQHK-UHFFFAOYSA-N amicarbazone Chemical compound CC(C)C1=NN(C(=O)NC(C)(C)C)C(=O)N1N ORFPWVRKFLOQHK-UHFFFAOYSA-N 0.000 abstract 1
- LVKBXDHACCFCTA-UHFFFAOYSA-N bencarbazone Chemical compound C1=C(C(N)=S)C(NS(=O)(=O)CC)=CC(N2C(N(C)C(=N2)C(F)(F)F)=O)=C1F LVKBXDHACCFCTA-UHFFFAOYSA-N 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 150000001721 carbon Chemical group 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000001153 fluoro group Chemical group F* 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- PMHURSZHKKJGBM-UHFFFAOYSA-N isoxaben Chemical compound O1N=C(C(C)(CC)CC)C=C1NC(=O)C1=C(OC)C=CC=C1OC PMHURSZHKKJGBM-UHFFFAOYSA-N 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- FKLQIONHGSFYJY-UHFFFAOYSA-N propan-2-yl 5-[4-bromo-1-methyl-5-(trifluoromethyl)pyrazol-3-yl]-2-chloro-4-fluorobenzoate Chemical compound C1=C(Cl)C(C(=O)OC(C)C)=CC(C=2C(=C(N(C)N=2)C(F)(F)F)Br)=C1F FKLQIONHGSFYJY-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 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 abstract 1
- IYMLUHWAJFXAQP-UHFFFAOYSA-N topramezone Chemical compound CC1=C(C(=O)C2=C(N(C)N=C2)O)C=CC(S(C)(=O)=O)=C1C1=NOCC1 IYMLUHWAJFXAQP-UHFFFAOYSA-N 0.000 abstract 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
El invento se refiere a una combinación de herbicidas, que contiene unos componentes (A) y (B), realizándose que (A)representa uno o varios compuestos o sus sales tomados del conjunto descrito por la fórmula general (I): en la que R1 representa un halógeno, de manera preferida fluoro o cloro, R2 significa hidrógeno y R3 significa hidroxilo o R2 y R3 tomados en común con el átomo de carbono, al que ellos están unidos, significan un grupo carbonilo C=O y R4 significa hidrógeno o metilo; y (B) significa uno o varios herbicidas tomados del conjunto que se compone de: (B1-1) benzofenap; (B1-2) pirazolinato; (B1-3) pirazoxifeno; (B1-4) piroxasulfona; (B1-5) topramezona; (B1-6) pirasulfotol; (B1-7) NC-310; (B2-1) piraflufeno; (B2-2) fluazolato; (B3-1) isourón; (B3-2) isoxaben; (B3-3) isoxaflutol; (B4-1) imazametabenz-metilo; (B4-2) imazamox; (B4-3) imazapic; (B4-4) imazapir; (B4-5) imazaquin; (B4-6) imazetapir; (B4-7) profluazol; (B5-1) metazol; (B5-2) oxadiargilo; (B5-3) oxadiazona; (B6-1) amicarbazona; (B6-2) carfentrazona; (B6-3) sulfentrazona; (B6-4) bencarbazona; (B6-5) ipfencarbazona; (B7-1) amitrol; (B7-2) paclobutrazol; (B7-3) uniconazol; (B7-4) cafenstrol; (B8-1) fentrazamida; (B8-2) F-5231.The invention relates to a combination of herbicides, which contains components (A) and (B), realizing that (A) represents one or more compounds or their salts taken from the set described by the general formula (I): in which R1 represents a halogen, preferably fluoro or chloro, R2 means hydrogen and R3 means hydroxyl or R2 and R3 taken in common with the carbon atom, to which they are attached, means a carbonyl group C = O and R4 means hydrogen or methyl; and (B) means one or more herbicides taken from the set consisting of: (B1-1) benzofenap; (B1-2) pyrazolinate; (B1-3) pyrazoxyphene; (B1-4) pyroxasulfone; (B1-5) topramezone; (B1-6) pyrasulfotol; (B1-7) NC-310; (B2-1) pyrefluphene; (B2-2) fluazolate; (B3-1) isouron; (B3-2) isoxaben; (B3-3) isoxaflutol; (B4-1) imazametabenz-methyl; (B4-2) imazamox; (B4-3) imazapic; (B4-4) imazapyr; (B4-5) Imazaquin; (B4-6) Imazetapyr; (B4-7) profluazole; (B5-1) metazole; (B5-2) oxadiargyl; (B5-3) oxadiazone; (B6-1) amicarbazone; (B6-2) carfentrazone; (B6-3) sulfentrazone; (B6-4) bencarbazone; (B6-5) ipfencarbazone; (B7-1) amitrole; (B7-2) paclobutrazol; (B7-3) uniconazole; (B7-4) cafenstrol; (B8-1) fentrazamide; (B8-2) F-5231.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ECSP11010821 ECSP11010821A (en) | 2011-02-11 | 2011-02-11 | Combination of herbicides with difluoromethanesulfonilanilides substituted with dimethoxytriazinyl |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ECSP11010821 ECSP11010821A (en) | 2011-02-11 | 2011-02-11 | Combination of herbicides with difluoromethanesulfonilanilides substituted with dimethoxytriazinyl |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ECSP11010821A true ECSP11010821A (en) | 2011-09-30 |
Family
ID=47790599
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ECSP11010821 ECSP11010821A (en) | 2011-02-11 | 2011-02-11 | Combination of herbicides with difluoromethanesulfonilanilides substituted with dimethoxytriazinyl |
Country Status (1)
| Country | Link |
|---|---|
| EC (1) | ECSP11010821A (en) |
-
2011
- 2011-02-11 EC ECSP11010821 patent/ECSP11010821A/en unknown
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