MA31790B1 - Combinaison herbicide - Google Patents
Combinaison herbicideInfo
- Publication number
- MA31790B1 MA31790B1 MA32791A MA32791A MA31790B1 MA 31790 B1 MA31790 B1 MA 31790B1 MA 32791 A MA32791 A MA 32791A MA 32791 A MA32791 A MA 32791A MA 31790 B1 MA31790 B1 MA 31790B1
- Authority
- MA
- Morocco
- Prior art keywords
- ion
- alkyl
- trifluormethyl
- methyl
- fizadiazole
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title abstract 3
- 230000002363 herbicidal effect Effects 0.000 title abstract 2
- -1 iron ion Chemical class 0.000 abstract 7
- 125000004429 atom Chemical group 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 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
- 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
- LNAZMLYBZCOSPN-UHFFFAOYSA-N 1-ethyl-3-[3-fluoro-5-[2-methyl-5-(trifluoromethyl)pyrazol-3-yl]oxyphenoxy]-5-(trifluoromethyl)pyrazole Chemical compound C1=C(C(F)(F)F)N(CC)N=C1OC1=CC(F)=CC(OC=2N(N=C(C=2)C(F)(F)F)C)=C1 LNAZMLYBZCOSPN-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
- DYEZIEPEFHQIGL-UHFFFAOYSA-N 3-[3-chloro-5-[2-methyl-5-(trifluoromethyl)pyrazol-3-yl]oxyphenoxy]-1-methyl-5-(trifluoromethyl)pyrazole Chemical compound CN1N=C(C(F)(F)F)C=C1OC1=CC(Cl)=CC(OC2=NN(C)C(=C2)C(F)(F)F)=C1 DYEZIEPEFHQIGL-UHFFFAOYSA-N 0.000 abstract 1
- TUZVYQPQVVAXGG-UHFFFAOYSA-N 3-[3-iodo-5-[2-methyl-5-(trifluoromethyl)pyrazol-3-yl]oxyphenoxy]-1-methyl-5-(trifluoromethyl)pyrazole Chemical compound CN1N=C(C(F)(F)F)C=C1OC1=CC(I)=CC(OC2=NN(C)C(=C2)C(F)(F)F)=C1 TUZVYQPQVVAXGG-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
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 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
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 abstract 1
- 239000005492 Carfentrazone-ethyl Substances 0.000 abstract 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
- 239000005566 Imazamox Substances 0.000 abstract 1
- XVOKUMIPKHGGTN-UHFFFAOYSA-N Imazethapyr Chemical compound OC(=O)C1=CC(CC)=CN=C1C1=NC(C)(C(C)C)C(=O)N1 XVOKUMIPKHGGTN-UHFFFAOYSA-N 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
- 239000005571 Isoxaflutole Substances 0.000 abstract 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 abstract 1
- JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 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
- NPYPAHLBTDXSSS-UHFFFAOYSA-N Potassium ion Chemical compound [K+] NPYPAHLBTDXSSS-UHFFFAOYSA-N 0.000 abstract 1
- 239000005605 Pyraflufen-ethyl Substances 0.000 abstract 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract 1
- 229910001413 alkali metal ion Inorganic materials 0.000 abstract 1
- 229910001420 alkaline earth metal ion Inorganic materials 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
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000000852 azido group Chemical group *N=[N+]=[N-] 0.000 abstract 1
- 150000003851 azoles Chemical class 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
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 239000011575 calcium Substances 0.000 abstract 1
- 229910001424 calcium ion Inorganic materials 0.000 abstract 1
- 150000001768 cations Chemical class 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 229910052802 copper Inorganic materials 0.000 abstract 1
- 239000010949 copper Substances 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- MLKCGVHIFJBRCD-UHFFFAOYSA-N ethyl 2-chloro-3-{2-chloro-5-[4-(difluoromethyl)-3-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]-4-fluorophenyl}propanoate Chemical group C1=C(Cl)C(CC(Cl)C(=O)OCC)=CC(N2C(N(C(F)F)C(C)=N2)=O)=C1F MLKCGVHIFJBRCD-UHFFFAOYSA-N 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 150000002391 heterocyclic compounds Chemical class 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 1
- 229910052742 iron Inorganic materials 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
- OYIKARCXOQLFHF-UHFFFAOYSA-N isoxaflutole Chemical compound CS(=O)(=O)C1=CC(C(F)(F)F)=CC=C1C(=O)C1=C(C2CC2)ON=C1 OYIKARCXOQLFHF-UHFFFAOYSA-N 0.000 abstract 1
- 229940088649 isoxaflutole Drugs 0.000 abstract 1
- 229910001416 lithium ion Inorganic materials 0.000 abstract 1
- 229910001425 magnesium ion Inorganic materials 0.000 abstract 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 229910001414 potassium ion Inorganic materials 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
- APTZNLHMIGJTEW-UHFFFAOYSA-N pyraflufen-ethyl Chemical group C1=C(Cl)C(OCC(=O)OCC)=CC(C=2C(=C(OC(F)F)N(C)N=2)Cl)=C1F APTZNLHMIGJTEW-UHFFFAOYSA-N 0.000 abstract 1
- DWSPRBSLSXQIEJ-UHFFFAOYSA-N pyrasulfotole Chemical compound CC1=NN(C)C(O)=C1C(=O)C1=CC=C(C(F)(F)F)C=C1S(C)(=O)=O DWSPRBSLSXQIEJ-UHFFFAOYSA-N 0.000 abstract 1
- ASRAWSBMDXVNLX-UHFFFAOYSA-N pyrazolynate Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=O)C=1C(C)=NN(C)C=1OS(=O)(=O)C1=CC=C(C)C=C1 ASRAWSBMDXVNLX-UHFFFAOYSA-N 0.000 abstract 1
- FKERUJTUOYLBKB-UHFFFAOYSA-N pyrazoxyfen Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=O)C=1C(C)=NN(C)C=1OCC(=O)C1=CC=CC=C1 FKERUJTUOYLBKB-UHFFFAOYSA-N 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 229910001415 sodium ion Inorganic materials 0.000 abstract 1
- 125000001424 substituent group Chemical group 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
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 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
- 229910001428 transition metal ion Inorganic materials 0.000 abstract 1
- 239000011701 zinc Substances 0.000 abstract 1
- 229910052725 zinc Inorganic materials 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
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
La présente invention concerne une combinaison herbicide contenant les constituants (a) et (b). (a) représente un ou plusieurs agents herbicides choisis dans le groupe comprenant le 2-iodo-n-[(4-méthoxy-6-méthyl-1,3,5-triazin-2-yl)carbamoyl]benzène sulfonamide et des composés de formule générale (i) dans laquelle le cation (m+) est : (a) un ion de métal alcalin, de préférence un ion de lithium, sodium, potassium; ou (b) un ion de métal alcalino-terreux, de préférence un ion de calcium ou magnésium; ou (c) un ion de métal de transition, de préférence un ion de manganèse, cuivre, zinc ou fer; ou (d) un ion ammonium, éventuellement un, deux, trois, voire les quatre atomes d'hydrogène étant substitués par des radicaux identiques ou différents choisis dans le groupe contenant (c1-c4)-alkyle, hydroxy- (c1-c4)-alkyle, (c3-c6)-cycloalkyle, (c1-c4)-alcoxy- c1-c4)-alkyle, hydroxy-(c1-c4)-alcoxy-( c1-c)-alkyle, (c1-c6) -mercaptoalkyle, phényle ou benzyle, les radicaux mentionnés précédemment étant éventuellement substitués par un ou plusieurs radicaux identiques ou différents choisis dans le groupe qui comprend un halogène tel que f, cl, br ou i, nitro, cyano, azido, (c1-c6)-aikyie, (c1-c6) haloalkyle, (c3-c6)-cycloalkyle, (c1-c6) -alcoxy, (c1-c6)-haloalcoxy et phényle, et respectivement deux substituants formant ensemble au niveau de l'atome de n éventuellement un cycle substitué ou non; ou (e) un ion phosphonium; ou (f) un ion sulfonium, de préférence tri-((c1-c4)-alkyle)- sulfonium; ou (g) un ion oxonium, de préférence tri-((c1-c4)-alkyle)-oxonium; ou (h) un composé ionique hétérocyclique annelé une ou plusieurs fois et/ou substitué par (c1-c4)-alkyle, saturé ou non / aromatique contenant n, comprenant 1-10 atomes de c dans le système cyclique. (b) représente un ou plusieurs agents herbicides choisis dans le groupe des azoles comprenant : benzofenap, pyrazolynate, pyrazoxyfène, pyroxasulfone, topramézone, pyrasulfotole, nc-310, 3-(3-chloro-5-{[1-méthyl-3- (trifluorméthyl)-1h-pyrazol-5-yl]oxy}phénoxy)-1-méthyl-5- (trifluorméthyl)-1 h-pyrazole, 3-(3-iodo-5-{[1-méthyl-3- (trifluorméthyl)-1h-pyrazol-5-yl]oxy}phénoxy)-1-méthyl-5-(trifluorméthyl) -1 h-pyrazole, 1-éthyl-3-(3-fluoro-5-{[1 -méthyl- 3-(trifluorméthyl)-1h-pyrazol-5-yl]oxy}phénoxy) -5-(trifluorméthyl)-1h-pyrazole, pyraflufène-éthyl, fluazolate, isouron, isoxaben, isoxaflutole,imazaméthabenzméthyle, imazamox, imazapic, imazapyr, imazaquine, imazéthapyr, syp-298, syp-300, méthazole, oxadiargyl, oxadiazone, amicarbazone, carfentrazone-éthyle, sulfentrazone, bencarbazone, ipfencarbazone, méthiozoline, amitrole, paclobutrazol, uniconazole, cafenstrole, fentrazamide, f-5231, pinoxaden.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07020858A EP2052615A1 (fr) | 2007-10-24 | 2007-10-24 | Combinaison d'herbicide |
| PCT/EP2008/008943 WO2009053054A2 (fr) | 2007-10-24 | 2008-10-22 | Combinaison herbicide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA31790B1 true MA31790B1 (fr) | 2010-10-01 |
Family
ID=39579983
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA32791A MA31790B1 (fr) | 2007-10-24 | 2010-04-23 | Combinaison herbicide |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US20100323894A1 (fr) |
| EP (2) | EP2052615A1 (fr) |
| JP (1) | JP2011500744A (fr) |
| CN (1) | CN101835380A (fr) |
| AR (1) | AR068959A1 (fr) |
| AU (1) | AU2008315604A1 (fr) |
| BR (1) | BRPI0818218A2 (fr) |
| CA (1) | CA2703576A1 (fr) |
| CL (1) | CL2008003146A1 (fr) |
| EA (1) | EA201000525A1 (fr) |
| MA (1) | MA31790B1 (fr) |
| TN (1) | TN2010000184A1 (fr) |
| WO (1) | WO2009053054A2 (fr) |
| ZA (1) | ZA201002566B (fr) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9832996B2 (en) | 2013-10-01 | 2017-12-05 | Marrone Bio Innovations, Inc. | Use of sarmentine and its analogues with an herbicide, and compositions thereof |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
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| US2670282A (en) | 1952-03-05 | 1954-02-23 | American Chem Paint Co | Plant growth regulation |
| FR1394774A (fr) | 1963-12-13 | 1965-04-09 | Rhone Poulenc Sa | Nouveaux dérivés de l'oxadiazolone et leur préparation |
| ES403445A1 (es) | 1971-06-02 | 1975-05-16 | Rhone Poulenc Sa | Procedimiento para la obtencion de derivados de la oxadia- zolona. |
| JPS5031039A (fr) | 1973-07-27 | 1975-03-27 | ||
| JPS5436648B2 (fr) | 1974-03-28 | 1979-11-10 | ||
| US4169719A (en) | 1976-04-07 | 1979-10-02 | E. I. Du Pont De Nemours And Co. | Herbicidal sulfonamides |
| CA1082189A (fr) | 1976-04-07 | 1980-07-22 | George Levitt | Sulfamides herbicides |
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| JPS6053018B2 (ja) | 1977-09-07 | 1985-11-22 | 住友化学工業株式会社 | アゾ−ル系化合物、その製造法および該化合物からなる殺菌剤 |
| US4798619A (en) | 1980-06-02 | 1989-01-17 | American Cyanamid Co. | 2-(2-imidazolin-2-yl)-pyridines and quinolines and use of said compounds as herbicidal agents |
| IL62794A0 (en) | 1980-06-02 | 1981-07-31 | American Cyanamid Co | Substituted nicotinic acid esters and salts thereof and their use as herbicidal agents |
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| US4636243A (en) | 1980-09-16 | 1987-01-13 | Eli Lilly And Company | Benzamides, compositions and agricultural method |
| DE3035554A1 (de) | 1980-09-20 | 1982-05-06 | Hoechst Ag, 6000 Frankfurt | Herbizide mittel |
| JPS5772903A (en) | 1980-10-27 | 1982-05-07 | Mitsubishi Petrochem Co Ltd | Pyrazole herbicide |
| US4629494A (en) | 1981-12-07 | 1986-12-16 | E. I. Du Pont De Nemours And Company | Herbicidal sulfonamides |
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| DE102005014638A1 (de) | 2005-03-31 | 2006-10-05 | Bayer Cropscience Gmbh | Substituierte Pyrazolyloxyphenylderivate als Herbizide |
| EP1717232A1 (fr) * | 2005-04-28 | 2006-11-02 | Bayer CropScience GmbH | Urées phénylsulfonyles ayant une activité herbicide |
| WO2007023719A1 (fr) | 2005-08-22 | 2007-03-01 | Kumiai Chemical Industry Co., Ltd. | Agent servant à réduire l'attaque chimique et composition herbicide produisant une attaque chimique réduite |
| WO2007023764A1 (fr) | 2005-08-26 | 2007-03-01 | Kumiai Chemical Industry Co., Ltd. | Agent servant à réduire les effets nocifs d’un herbicide et composition d’herbicide ayant des effets nocifs réduits |
-
2007
- 2007-10-24 EP EP07020858A patent/EP2052615A1/fr not_active Withdrawn
-
2008
- 2008-10-22 EA EA201000525A patent/EA201000525A1/ru unknown
- 2008-10-22 US US12/739,098 patent/US20100323894A1/en not_active Abandoned
- 2008-10-22 EP EP08843022A patent/EP2205095A2/fr not_active Withdrawn
- 2008-10-22 CN CN200880113222A patent/CN101835380A/zh active Pending
- 2008-10-22 JP JP2010530338A patent/JP2011500744A/ja active Pending
- 2008-10-22 CA CA2703576A patent/CA2703576A1/fr not_active Abandoned
- 2008-10-22 AR ARP080104599A patent/AR068959A1/es unknown
- 2008-10-22 BR BRPI0818218-3A2A patent/BRPI0818218A2/pt not_active Application Discontinuation
- 2008-10-22 WO PCT/EP2008/008943 patent/WO2009053054A2/fr not_active Ceased
- 2008-10-22 AU AU2008315604A patent/AU2008315604A1/en not_active Abandoned
- 2008-10-24 CL CL2008003146A patent/CL2008003146A1/es unknown
-
2010
- 2010-04-13 ZA ZA2010/02566A patent/ZA201002566B/en unknown
- 2010-04-23 TN TN2010000184A patent/TN2010000184A1/fr unknown
- 2010-04-23 MA MA32791A patent/MA31790B1/fr unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BRPI0818218A2 (pt) | 2014-10-07 |
| WO2009053054A3 (fr) | 2010-05-20 |
| WO2009053054A2 (fr) | 2009-04-30 |
| EP2052615A1 (fr) | 2009-04-29 |
| CN101835380A (zh) | 2010-09-15 |
| TN2010000184A1 (en) | 2011-11-11 |
| CL2008003146A1 (es) | 2009-03-06 |
| JP2011500744A (ja) | 2011-01-06 |
| ZA201002566B (en) | 2011-03-30 |
| US20100323894A1 (en) | 2010-12-23 |
| CA2703576A1 (fr) | 2009-04-30 |
| AU2008315604A1 (en) | 2009-04-30 |
| EP2205095A2 (fr) | 2010-07-14 |
| AR068959A1 (es) | 2009-12-16 |
| EA201000525A1 (ru) | 2010-10-29 |
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