BRPI0510262B1 - Composição herbicida, e, método de combater ervas danihas e gramíneas daninhas em colheitas de plantas úteis - Google Patents
Composição herbicida, e, método de combater ervas danihas e gramíneas daninhas em colheitas de plantas úteis Download PDFInfo
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- BRPI0510262B1 BRPI0510262B1 BRPI0510262-6A BRPI0510262A BRPI0510262B1 BR PI0510262 B1 BRPI0510262 B1 BR PI0510262B1 BR PI0510262 A BRPI0510262 A BR PI0510262A BR PI0510262 B1 BRPI0510262 B1 BR PI0510262B1
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- Brazil
- Prior art keywords
- formula
- compound
- alkyl
- substituted
- ethyl
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- 239000000203 mixture Substances 0.000 title claims abstract description 90
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 39
- 241000196324 Embryophyta Species 0.000 title claims description 31
- 238000000034 method Methods 0.000 title claims description 20
- 150000001875 compounds Chemical class 0.000 claims abstract description 473
- -1 C 1 -C 8 alkylalkyl Chemical group 0.000 claims description 107
- 239000003223 protective agent Substances 0.000 claims description 53
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 47
- 239000001257 hydrogen Substances 0.000 claims description 44
- 229910052739 hydrogen Inorganic materials 0.000 claims description 44
- 239000004009 herbicide Substances 0.000 claims description 41
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 34
- PFJJMJDEVDLPNE-UHFFFAOYSA-N Benoxacor Chemical compound C1=CC=C2N(C(=O)C(Cl)Cl)C(C)COC2=C1 PFJJMJDEVDLPNE-UHFFFAOYSA-N 0.000 claims description 31
- 125000000217 alkyl group Chemical group 0.000 claims description 29
- 229910052736 halogen Inorganic materials 0.000 claims description 29
- 150000002367 halogens Chemical class 0.000 claims description 29
- 125000001072 heteroaryl group Chemical group 0.000 claims description 28
- 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 claims description 26
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 21
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 20
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 18
- 240000008042 Zea mays Species 0.000 claims description 18
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims description 18
- 244000038559 crop plants Species 0.000 claims description 18
- YRMLFORXOOIJDR-UHFFFAOYSA-N Dichlormid Chemical compound ClC(Cl)C(=O)N(CC=C)CC=C YRMLFORXOOIJDR-UHFFFAOYSA-N 0.000 claims description 16
- 125000004432 carbon atom Chemical group C* 0.000 claims description 16
- 125000003118 aryl group Chemical group 0.000 claims description 15
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 14
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims description 13
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 claims description 10
- 125000004414 alkyl thio group Chemical group 0.000 claims description 10
- 229910052799 carbon Inorganic materials 0.000 claims description 10
- 235000009973 maize Nutrition 0.000 claims description 10
- 125000005115 alkyl carbamoyl group Chemical group 0.000 claims description 9
- 229910052760 oxygen Inorganic materials 0.000 claims description 9
- 239000001301 oxygen Substances 0.000 claims description 9
- 229910052757 nitrogen Inorganic materials 0.000 claims description 8
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 7
- 125000004434 sulfur atom Chemical group 0.000 claims description 7
- 240000005979 Hordeum vulgare Species 0.000 claims description 6
- 235000007340 Hordeum vulgare Nutrition 0.000 claims description 6
- 125000002619 bicyclic group Chemical group 0.000 claims description 6
- 125000005842 heteroatom Chemical group 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- 125000002950 monocyclic group Chemical group 0.000 claims description 6
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 6
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 claims description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 5
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 5
- 239000013543 active substance Substances 0.000 claims description 3
- 125000004692 haloalkylcarbonyl group Chemical group 0.000 claims description 3
- 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 description 3
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 2
- 125000001541 3-thienyl group Chemical group S1C([H])=C([*])C([H])=C1[H] 0.000 claims description 2
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims description 2
- 125000001188 haloalkyl group Chemical group 0.000 claims description 2
- 125000001786 isothiazolyl group Chemical group 0.000 claims description 2
- 125000004498 isoxazol-4-yl group Chemical group O1N=CC(=C1)* 0.000 claims description 2
- 125000000842 isoxazolyl group Chemical group 0.000 claims description 2
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims description 2
- 125000004497 pyrazol-5-yl group Chemical group N1N=CC=C1* 0.000 claims description 2
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 2
- 125000004076 pyridyl group Chemical group 0.000 claims description 2
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 2
- 125000001544 thienyl group Chemical group 0.000 claims description 2
- 244000045561 useful plants Species 0.000 claims 2
- 125000004528 pyrimidin-5-yl group Chemical group N1=CN=CC(=C1)* 0.000 claims 1
- GRSMWKLPSNHDHA-UHFFFAOYSA-N Naphthalic anhydride Chemical compound C1=CC(C(=O)OC2=O)=C3C2=CC=CC3=C1 GRSMWKLPSNHDHA-UHFFFAOYSA-N 0.000 description 23
- 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 description 23
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 22
- 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 description 22
- 239000000654 additive Substances 0.000 description 19
- 239000004094 surface-active agent Substances 0.000 description 17
- 125000003545 alkoxy group Chemical group 0.000 description 15
- 238000009472 formulation Methods 0.000 description 15
- 239000002253 acid Substances 0.000 description 14
- WFVUIONFJOAYPK-KAMYIIQDSA-N Oxabetrinil Chemical compound C=1C=CC=CC=1C(/C#N)=N\OCC1OCCO1 WFVUIONFJOAYPK-KAMYIIQDSA-N 0.000 description 13
- 239000000126 substance Substances 0.000 description 13
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 12
- 229910052782 aluminium Inorganic materials 0.000 description 12
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 12
- 239000003921 oil Substances 0.000 description 12
- 235000019198 oils Nutrition 0.000 description 12
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 12
- 125000001453 quaternary ammonium group Chemical group 0.000 description 12
- 239000011734 sodium Substances 0.000 description 12
- 239000007787 solid Substances 0.000 description 12
- BUNHNNQIXNPQAZ-UHFFFAOYSA-N 2-methoxy-n-[4-(propan-2-ylcarbamoyl)phenyl]sulfonylbenzamide Chemical compound COC1=CC=CC=C1C(=O)NS(=O)(=O)C1=CC=C(C(=O)NC(C)C)C=C1 BUNHNNQIXNPQAZ-UHFFFAOYSA-N 0.000 description 11
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 11
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 11
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 11
- 239000011248 coating agent Substances 0.000 description 11
- 238000000576 coating method Methods 0.000 description 11
- 229910052742 iron Inorganic materials 0.000 description 11
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 description 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
- NRFQZTCQAYEXEE-UHFFFAOYSA-N Fenclorim Chemical compound ClC1=CC(Cl)=NC(C=2C=CC=CC=2)=N1 NRFQZTCQAYEXEE-UHFFFAOYSA-N 0.000 description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 10
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 10
- 230000000996 additive effect Effects 0.000 description 9
- 238000002156 mixing Methods 0.000 description 9
- 229910052708 sodium Inorganic materials 0.000 description 9
- 239000002689 soil Substances 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 description 8
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 8
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 8
- 150000001768 cations Chemical class 0.000 description 8
- 229910052802 copper Inorganic materials 0.000 description 8
- 239000010949 copper Substances 0.000 description 8
- 235000005822 corn Nutrition 0.000 description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 8
- 239000007788 liquid Substances 0.000 description 8
- 239000003981 vehicle Substances 0.000 description 8
- 239000012141 concentrate Substances 0.000 description 7
- 239000000839 emulsion Substances 0.000 description 7
- 239000008187 granular material Substances 0.000 description 7
- 229910052717 sulfur Inorganic materials 0.000 description 7
- 229920000742 Cotton Polymers 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 241000209140 Triticum Species 0.000 description 6
- 235000021307 Triticum Nutrition 0.000 description 6
- 150000001342 alkaline earth metals Chemical class 0.000 description 6
- 125000003342 alkenyl group Chemical group 0.000 description 6
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 description 6
- 239000011575 calcium Substances 0.000 description 6
- 229910052791 calcium Inorganic materials 0.000 description 6
- OAWUUPVZMNKZRY-UHFFFAOYSA-N cyprosulfamide Chemical compound COC1=CC=CC=C1C(=O)NS(=O)(=O)C1=CC=C(C(=O)NC2CC2)C=C1 OAWUUPVZMNKZRY-UHFFFAOYSA-N 0.000 description 6
- 125000006678 phenoxycarbonyl group Chemical group 0.000 description 6
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 description 6
- 229920001223 polyethylene glycol Polymers 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 239000004546 suspension concentrate Substances 0.000 description 6
- 239000004563 wettable powder Substances 0.000 description 6
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 description 5
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 description 5
- 125000006766 (C2-C6) alkynyloxy group Chemical group 0.000 description 5
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 description 5
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 5
- 244000299507 Gossypium hirsutum Species 0.000 description 5
- QYPPRTNMGCREIM-UHFFFAOYSA-N Monomethylarsonic acid Natural products C[As](O)(O)=O QYPPRTNMGCREIM-UHFFFAOYSA-N 0.000 description 5
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 5
- 125000004390 alkyl sulfonyl group Chemical group 0.000 description 5
- 230000009931 harmful effect Effects 0.000 description 5
- UQDUPQYQJKYHQI-UHFFFAOYSA-N methyl laurate Chemical compound CCCCCCCCCCCC(=O)OC UQDUPQYQJKYHQI-UHFFFAOYSA-N 0.000 description 5
- 239000003094 microcapsule Substances 0.000 description 5
- 239000007921 spray Substances 0.000 description 5
- GBXQPDCOMJJCMJ-UHFFFAOYSA-M trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;bromide Chemical compound [Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C GBXQPDCOMJJCMJ-UHFFFAOYSA-M 0.000 description 5
- 235000015112 vegetable and seed oil Nutrition 0.000 description 5
- 239000008158 vegetable oil Substances 0.000 description 5
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 description 4
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 4
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 4
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 4
- 235000010469 Glycine max Nutrition 0.000 description 4
- 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 description 4
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 4
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 4
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- 125000004183 alkoxy alkyl group Chemical group 0.000 description 4
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- OGGXGZAMXPVRFZ-UHFFFAOYSA-N dimethylarsinic acid Chemical compound C[As](C)(O)=O OGGXGZAMXPVRFZ-UHFFFAOYSA-N 0.000 description 4
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- 239000006185 dispersion Substances 0.000 description 4
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- 239000011777 magnesium Substances 0.000 description 4
- 229910052749 magnesium Inorganic materials 0.000 description 4
- QYDYPVFESGNLHU-KHPPLWFESA-N methyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC QYDYPVFESGNLHU-KHPPLWFESA-N 0.000 description 4
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- 239000011591 potassium Substances 0.000 description 4
- 229910052700 potassium Inorganic materials 0.000 description 4
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- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 4
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- 231100000765 toxin Toxicity 0.000 description 4
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- 125000003320 C2-C6 alkenyloxy group Chemical group 0.000 description 3
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Classifications
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- 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
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)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH00767/04 | 2004-04-30 | ||
| CH7672004 | 2004-04-30 | ||
| PCT/EP2005/004610 WO2005104848A1 (en) | 2004-04-30 | 2005-04-29 | Herbicidal composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| BRPI0510262A BRPI0510262A (pt) | 2007-10-30 |
| BRPI0510262B1 true BRPI0510262B1 (pt) | 2014-04-29 |
Family
ID=35044966
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BRPI0510262-6A BRPI0510262B1 (pt) | 2004-04-30 | 2005-04-29 | Composição herbicida, e, método de combater ervas danihas e gramíneas daninhas em colheitas de plantas úteis |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US8404618B2 (enExample) |
| EP (1) | EP1755397B1 (enExample) |
| JP (2) | JP4980209B2 (enExample) |
| AT (1) | ATE383074T1 (enExample) |
| AU (1) | AU2005237241B2 (enExample) |
| BR (1) | BRPI0510262B1 (enExample) |
| CA (2) | CA2829979A1 (enExample) |
| DE (1) | DE602005004283T2 (enExample) |
| ES (1) | ES2297709T3 (enExample) |
| PL (1) | PL1755397T3 (enExample) |
| WO (1) | WO2005104848A1 (enExample) |
| ZA (1) | ZA200608416B (enExample) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1755397B1 (en) * | 2004-04-30 | 2008-01-09 | Syngenta Participations AG | Herbicidal composition |
| BRPI0516442A (pt) | 2004-10-05 | 2008-09-02 | Syngenta Ltd | composto, processo para a preparação de um composto, composição herbicida, e, método para controlar gramìneas e ervas daninhas em safras de plantas úteis |
| MY144905A (en) * | 2005-03-17 | 2011-11-30 | Basf Ag | Herbicidal compositions based on 3-phenyluracils and 3-sulfonylisoxazolines |
| GB0505645D0 (en) | 2005-03-18 | 2005-04-27 | Syngenta Participations Ag | Herbicidal composition |
| WO2007003296A1 (de) * | 2005-07-06 | 2007-01-11 | Bayer Cropscience Ag | Herbizid-safener-kombination |
| WO2007006409A2 (de) * | 2005-07-07 | 2007-01-18 | Bayer Cropscience Ag | Herbizid-safener-kombination |
| GB0526044D0 (en) * | 2005-12-21 | 2006-02-01 | Syngenta Ltd | Novel herbicides |
| GB0603891D0 (en) * | 2006-02-27 | 2006-04-05 | Syngenta Ltd | Novel herbicides |
| WO2007147828A1 (en) * | 2006-06-20 | 2007-12-27 | Basf Se | Herbicidal compositions comprising a 3-heterocyclyl-substituted benzoyl compound |
| AR062587A1 (es) * | 2006-08-30 | 2008-11-19 | Dow Agrosciences Llc | Composiciones agricolamente utiles |
| US8110530B2 (en) | 2006-12-21 | 2012-02-07 | Kumiai Chemical Industry Co., Ltd. | Herbicidal composition |
| EP2065373A1 (de) | 2007-11-30 | 2009-06-03 | Bayer CropScience AG | Chirale 3-(Benzylsulfinyl)-5,5-dimethyl-4,5-dihydroisoxazol-Derivate und 5,5-Dimethyl-3-[(1H-pyrazol-4-ylmethyl) sulfinyl]-4,5-dihydroisoxazol-Derivate, Verfahren zu deren Herstellung sowie deren Verwendung als Herbizide und Pflanzenwachstumsregulatoren |
| EP2092825A1 (de) | 2008-02-21 | 2009-08-26 | Bayer CropScience Aktiengesellschaft | Herbizid-Kombinationen enthaltend ein Herbizid der Klasse der Diamino-s-triazine |
| MX2010009299A (es) * | 2008-03-11 | 2010-09-14 | Basf Se | Composiciones herbicidas que comprenden piroxasulfona. |
| TW200944127A (en) | 2008-03-14 | 2009-11-01 | Basf Se | Herbicidal compositions comprising pyroxasulfone |
| BRPI0908162A2 (pt) * | 2008-03-20 | 2015-08-11 | Basf Se | Composição herbicida, uso de uma composição, método para controlar vegetação indesejavel, e, formulação herbicida |
| JP5927055B2 (ja) | 2011-06-24 | 2016-05-25 | 石原産業株式会社 | 除草組成物 |
| JP5659191B2 (ja) * | 2012-05-16 | 2015-01-28 | 学校法人同志社 | 複素環化合物、酸化触媒及びその使用 |
| UA117810C2 (uk) | 2012-05-24 | 2018-10-10 | Байєр Кропсайєнс Акцієнгезелльшафт | Гербіцидні композиції, які містять n-(тетразол-5-іл)арилкарбоксаміди |
| UA118765C2 (uk) | 2013-08-09 | 2019-03-11 | Байєр Кропсайєнс Акцієнгезелльшафт | Третинні гербіцидні комбінації, що містять дві сульфонілсечовини |
| UA120916C2 (uk) | 2013-10-25 | 2020-03-10 | Байєр Кропсайєнс Акцієнгезелльшафт | Гербіцидні композиції, що містять аміди n-(1,3,4-оксадіазол-2-іл)-арилкарбонової кислоти |
| AP2016009412A0 (en) * | 2014-02-28 | 2016-08-31 | Kumiai Chemical Industry Co | Agrochemical composition for foliage treatment |
| EP3732963A1 (en) * | 2015-08-07 | 2020-11-04 | Bayer CropScience Aktiengesellschaft | New uses of 2-(2,4-dichlorophenyl)methyl-4,4-dimethyl-3-isoxazolidone as foliar herbicide |
| JP6542606B2 (ja) * | 2015-08-18 | 2019-07-10 | クミアイ化学工業株式会社 | 農薬組成物及びその使用法 |
| CN108294016A (zh) * | 2018-02-02 | 2018-07-20 | 河北中天邦正生物科技股份公司 | 一种农药组合物及其应用 |
| AU2020300922C1 (en) | 2019-10-31 | 2024-04-18 | Kumiai Chemical Industry Co., Ltd. | Process For Producing Herbicide And Intermediate Thereof |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3810838B2 (ja) * | 1994-12-12 | 2006-08-16 | 三共アグロ株式会社 | 除草性イソオキサゾリン誘導体 |
| JPH08217611A (ja) * | 1995-02-15 | 1996-08-27 | Idemitsu Kosan Co Ltd | 農薬による作物への薬害軽減剤 |
| JPH09328483A (ja) * | 1996-06-11 | 1997-12-22 | Sankyo Co Ltd | 除草性イソオキサゾリン誘導体 |
| EP1089628A1 (de) * | 1998-06-26 | 2001-04-11 | Novartis Pharma AG. | Herbizides mittel |
| IL147651A0 (en) * | 1999-08-10 | 2002-08-14 | Ihara Chemical Ind Co | Isoxazoline derivative and herbicide containing the same as the active ingredient |
| US6555499B1 (en) * | 1999-09-07 | 2003-04-29 | Syngenta Crop Protection, Inc. | Herbicide agent |
| JP4465133B2 (ja) * | 2001-02-08 | 2010-05-19 | クミアイ化学工業株式会社 | イソオキサゾリン誘導体及びこれを有効成分とする除草剤 |
| JP4317445B2 (ja) * | 2001-06-21 | 2009-08-19 | クミアイ化学工業株式会社 | イソオキサゾリン誘導体及び除草剤 |
| JP2004002324A (ja) * | 2002-03-22 | 2004-01-08 | Kumiai Chem Ind Co Ltd | 除草剤組成物 |
| UA78071C2 (en) | 2002-08-07 | 2007-02-15 | Kumiai Chemical Industry Co | Herbicidal composition |
| EP1755397B1 (en) * | 2004-04-30 | 2008-01-09 | Syngenta Participations AG | Herbicidal composition |
-
2005
- 2005-04-29 EP EP05741054A patent/EP1755397B1/en not_active Expired - Lifetime
- 2005-04-29 JP JP2007509975A patent/JP4980209B2/ja not_active Expired - Fee Related
- 2005-04-29 AT AT05741054T patent/ATE383074T1/de not_active IP Right Cessation
- 2005-04-29 WO PCT/EP2005/004610 patent/WO2005104848A1/en not_active Ceased
- 2005-04-29 PL PL05741054T patent/PL1755397T3/pl unknown
- 2005-04-29 DE DE602005004283T patent/DE602005004283T2/de not_active Expired - Lifetime
- 2005-04-29 AU AU2005237241A patent/AU2005237241B2/en not_active Expired
- 2005-04-29 BR BRPI0510262-6A patent/BRPI0510262B1/pt not_active IP Right Cessation
- 2005-04-29 US US11/568,326 patent/US8404618B2/en active Active
- 2005-04-29 ES ES05741054T patent/ES2297709T3/es not_active Expired - Lifetime
- 2005-04-29 CA CA2829979A patent/CA2829979A1/en not_active Abandoned
- 2005-04-29 CA CA2563218A patent/CA2563218C/en not_active Expired - Fee Related
-
2006
- 2006-10-09 ZA ZA200608416A patent/ZA200608416B/xx unknown
-
2011
- 2011-09-07 JP JP2011194494A patent/JP2012036191A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| PL1755397T3 (pl) | 2008-06-30 |
| JP2007535513A (ja) | 2007-12-06 |
| EP1755397A1 (en) | 2007-02-28 |
| CA2563218A1 (en) | 2005-11-10 |
| EP1755397B1 (en) | 2008-01-09 |
| CA2563218C (en) | 2013-12-24 |
| ZA200608416B (en) | 2008-11-26 |
| AU2005237241A1 (en) | 2005-11-10 |
| US8404618B2 (en) | 2013-03-26 |
| CA2829979A1 (en) | 2005-11-10 |
| JP2012036191A (ja) | 2012-02-23 |
| AU2005237241B2 (en) | 2011-04-07 |
| BRPI0510262A (pt) | 2007-10-30 |
| DE602005004283D1 (de) | 2008-02-21 |
| ES2297709T3 (es) | 2008-05-01 |
| US20070259786A1 (en) | 2007-11-08 |
| JP4980209B2 (ja) | 2012-07-18 |
| WO2005104848A1 (en) | 2005-11-10 |
| DE602005004283T2 (de) | 2009-01-15 |
| ATE383074T1 (de) | 2008-01-15 |
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| Date | Code | Title | Description |
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| B06A | Patent application procedure suspended [chapter 6.1 patent gazette] | ||
| B09A | Decision: intention to grant [chapter 9.1 patent gazette] | ||
| B16A | Patent or certificate of addition of invention granted [chapter 16.1 patent gazette] |
Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 29/04/2005, OBSERVADAS AS CONDICOES LEGAIS. |
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| B21F | Lapse acc. art. 78, item iv - on non-payment of the annual fees in time |
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| B24J | Lapse because of non-payment of annual fees (definitively: art 78 iv lpi, resolution 113/2013 art. 12) |
Free format text: EM VIRTUDE DA EXTINCAO PUBLICADA NA RPI 2385 DE 20-09-2016 E CONSIDERANDO AUSENCIA DE MANIFESTACAO DENTRO DOS PRAZOS LEGAIS, INFORMO QUE CABE SER MANTIDA A EXTINCAO DA PATENTE E SEUS CERTIFICADOS, CONFORME O DISPOSTO NO ARTIGO 12, DA RESOLUCAO 113/2013. |