JP2007535513A5 - - Google Patents
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- Publication number
- JP2007535513A5 JP2007535513A5 JP2007509975A JP2007509975A JP2007535513A5 JP 2007535513 A5 JP2007535513 A5 JP 2007535513A5 JP 2007509975 A JP2007509975 A JP 2007509975A JP 2007509975 A JP2007509975 A JP 2007509975A JP 2007535513 A5 JP2007535513 A5 JP 2007535513A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- substituted
- hydrogen
- alkoxy
- cycloalkyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 125000000217 alkyl group Chemical group 0.000 claims 40
- 229910052739 hydrogen Inorganic materials 0.000 claims 32
- 239000001257 hydrogen Substances 0.000 claims 32
- -1 benzyloxy, amino Chemical group 0.000 claims 27
- 239000000203 mixture Substances 0.000 claims 22
- 150000002431 hydrogen Chemical class 0.000 claims 21
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 17
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 17
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims 16
- 229910052736 halogen Inorganic materials 0.000 claims 15
- 150000002367 halogens Chemical class 0.000 claims 15
- 150000001875 compounds Chemical class 0.000 claims 14
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 11
- 125000003342 alkenyl group Chemical group 0.000 claims 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 8
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims 8
- 229910052783 alkali metal Inorganic materials 0.000 claims 8
- 150000001340 alkali metals Chemical class 0.000 claims 8
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims 8
- 150000001342 alkaline earth metals Chemical class 0.000 claims 8
- 125000003302 alkenyloxy group Chemical group 0.000 claims 8
- 125000003545 alkoxy group Chemical group 0.000 claims 8
- 229910052782 aluminium Inorganic materials 0.000 claims 8
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims 8
- 150000001768 cations Chemical class 0.000 claims 8
- 229910052802 copper Inorganic materials 0.000 claims 8
- 239000010949 copper Substances 0.000 claims 8
- 230000002363 herbicidal effect Effects 0.000 claims 8
- 229910052742 iron Inorganic materials 0.000 claims 8
- 238000000034 method Methods 0.000 claims 8
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 claims 8
- 125000001453 quaternary ammonium group Chemical group 0.000 claims 8
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 claims 8
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 7
- 125000005115 alkyl carbamoyl group Chemical group 0.000 claims 7
- 125000000304 alkynyl group Chemical group 0.000 claims 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 6
- 229910052799 carbon Inorganic materials 0.000 claims 6
- 125000004432 carbon atom Chemical group C* 0.000 claims 6
- 239000004009 herbicide Substances 0.000 claims 6
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims 6
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims 5
- GMBRUAIJEFRHFQ-UHFFFAOYSA-N Fenchlorazole-ethyl Chemical group N1=C(C(=O)OCC)N=C(C(Cl)(Cl)Cl)N1C1=CC=C(Cl)C=C1Cl GMBRUAIJEFRHFQ-UHFFFAOYSA-N 0.000 claims 5
- 125000004093 cyano group Chemical group *C#N 0.000 claims 5
- OPGCOAPTHCZZIW-UHFFFAOYSA-N diethyl 1-(2,4-dichlorophenyl)-5-methyl-4h-pyrazole-3,5-dicarboxylate Chemical group CCOC(=O)C1(C)CC(C(=O)OCC)=NN1C1=CC=C(Cl)C=C1Cl OPGCOAPTHCZZIW-UHFFFAOYSA-N 0.000 claims 5
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 claims 4
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 4
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 4
- 125000004414 alkyl thio group Chemical group 0.000 claims 4
- 125000003118 aryl group Chemical group 0.000 claims 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 4
- 229910052760 oxygen Inorganic materials 0.000 claims 4
- 239000001301 oxygen Substances 0.000 claims 4
- 244000045561 useful plants Species 0.000 claims 4
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 3
- 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 claims 3
- GRSMWKLPSNHDHA-UHFFFAOYSA-N Naphthalic anhydride Chemical compound C1=CC(C(=O)OC2=O)=C3C2=CC=CC3=C1 GRSMWKLPSNHDHA-UHFFFAOYSA-N 0.000 claims 3
- 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 claims 3
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 3
- 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 claims 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 229910052757 nitrogen Inorganic materials 0.000 claims 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 3
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims 2
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 2
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims 2
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 2
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 2
- 125000006766 (C2-C6) alkynyloxy group Chemical group 0.000 claims 2
- 125000003320 C2-C6 alkenyloxy group Chemical group 0.000 claims 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 2
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims 2
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 claims 2
- 241000196324 Embryophyta Species 0.000 claims 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 2
- 240000008042 Zea mays Species 0.000 claims 2
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 claims 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims 2
- 125000003282 alkyl amino group Chemical group 0.000 claims 2
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 2
- 125000004656 alkyl sulfonylamino group Chemical group 0.000 claims 2
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 claims 2
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 claims 2
- 150000003863 ammonium salts Chemical class 0.000 claims 2
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 claims 2
- 125000002619 bicyclic group Chemical group 0.000 claims 2
- 159000000007 calcium salts Chemical class 0.000 claims 2
- 235000005822 corn Nutrition 0.000 claims 2
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 2
- 125000005842 heteroatom Chemical group 0.000 claims 2
- 150000002505 iron Chemical class 0.000 claims 2
- 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 claims 2
- 229910003002 lithium salt Inorganic materials 0.000 claims 2
- 159000000002 lithium salts Chemical class 0.000 claims 2
- 159000000003 magnesium salts Chemical class 0.000 claims 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 2
- 125000002950 monocyclic group Chemical group 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 2
- 125000006678 phenoxycarbonyl group Chemical group 0.000 claims 2
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 claims 2
- 150000004714 phosphonium salts Chemical class 0.000 claims 2
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 claims 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims 2
- 159000000000 sodium salts Chemical class 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- 239000011593 sulfur Substances 0.000 claims 2
- 125000004434 sulfur atom Chemical group 0.000 claims 2
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims 1
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims 1
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 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 claims 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 claims 1
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims 1
- 125000001541 3-thienyl group Chemical group S1C([H])=C([*])C([H])=C1[H] 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- 240000005979 Hordeum vulgare Species 0.000 claims 1
- 235000007340 Hordeum vulgare Nutrition 0.000 claims 1
- 241000209504 Poaceae Species 0.000 claims 1
- 241000209140 Triticum Species 0.000 claims 1
- 235000021307 Triticum Nutrition 0.000 claims 1
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- 230000003042 antagnostic effect Effects 0.000 claims 1
- 239000005557 antagonist Substances 0.000 claims 1
- 125000000043 benzamido group Chemical group [H]N([*])C(=O)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 1
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 1
- 125000001188 haloalkyl group Chemical group 0.000 claims 1
- 125000004440 haloalkylsulfinyl group Chemical group 0.000 claims 1
- 125000001072 heteroaryl group Chemical group 0.000 claims 1
- 125000004500 isothiazol-4-yl group Chemical group S1N=CC(=C1)* 0.000 claims 1
- 125000001786 isothiazolyl group Chemical group 0.000 claims 1
- 125000004498 isoxazol-4-yl group Chemical group O1N=CC(=C1)* 0.000 claims 1
- 125000000842 isoxazolyl group Chemical group 0.000 claims 1
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 claims 1
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims 1
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims 1
- 125000004497 pyrazol-5-yl group Chemical group N1N=CC=C1* 0.000 claims 1
- 125000003226 pyrazolyl group Chemical group 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 125000004528 pyrimidin-5-yl group Chemical group N1=CN=CC(=C1)* 0.000 claims 1
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
- 125000003396 thiol group Chemical class [H]S* 0.000 claims 1
- 0 *OC(C(C1)=NOC1(c1ccccc1)c1ccccc1)=O Chemical compound *OC(C(C1)=NOC1(c1ccccc1)c1ccccc1)=O 0.000 description 2
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH7672004 | 2004-04-30 | ||
| CH00767/04 | 2004-04-30 | ||
| PCT/EP2005/004610 WO2005104848A1 (en) | 2004-04-30 | 2005-04-29 | Herbicidal composition |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011194494A Division JP2012036191A (ja) | 2004-04-30 | 2011-09-07 | 除草剤組成物 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2007535513A JP2007535513A (ja) | 2007-12-06 |
| JP2007535513A5 true JP2007535513A5 (enExample) | 2010-07-22 |
| JP4980209B2 JP4980209B2 (ja) | 2012-07-18 |
Family
ID=35044966
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007509975A Expired - Fee Related JP4980209B2 (ja) | 2004-04-30 | 2005-04-29 | 除草剤組成物 |
| JP2011194494A Pending JP2012036191A (ja) | 2004-04-30 | 2011-09-07 | 除草剤組成物 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011194494A Pending JP2012036191A (ja) | 2004-04-30 | 2011-09-07 | 除草剤組成物 |
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 |
| PL1799657T3 (pl) | 2004-10-05 | 2010-05-31 | Syngenta Ltd | Pochodne izoksazoliny i ich zastosowanie jako herbicydów |
| 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 |
| RS53542B1 (sr) * | 2008-03-11 | 2015-02-27 | Basf Se | Herbicidne kompozicije koje sadrže piroksasulfon |
| TW200944127A (en) | 2008-03-14 | 2009-11-01 | Basf Se | Herbicidal compositions comprising pyroxasulfone |
| MY155253A (en) * | 2008-03-20 | 2015-09-30 | Basf Se | Herbicidal compositions comprising pyroxasulfone iv |
| 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 |
| EP2854538B1 (de) | 2012-05-24 | 2017-05-03 | Bayer CropScience AG | Herbizide zusammensetzungen enthaltend n-(tetrazol-5-yl)arylcarbonsäureamide |
| UA118765C2 (uk) | 2013-08-09 | 2019-03-11 | Байєр Кропсайєнс Акцієнгезелльшафт | Третинні гербіцидні комбінації, що містять дві сульфонілсечовини |
| CA2928243C (en) | 2013-10-25 | 2021-11-30 | Bayer Cropscience Aktiengesellschaft | Herbicidal compositions containing n-(1,3,4-oxadiazol-2-yl)-aryl carboxylic acid amides |
| CN106028810A (zh) * | 2014-02-28 | 2016-10-12 | 组合化学工业株式会社 | 茎叶处理用农药组合物 |
| PL3331363T3 (pl) * | 2015-08-07 | 2022-04-11 | Fmc Corporation | Nowe zastosowania 2-(2,4-dichlorofenylo)metylo-4,4-dimetylo-3-izoksazolidonu jako herbicydu dolistnego |
| 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 |
| CN113749106A (zh) * | 2018-02-02 | 2021-12-07 | 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 |
| KR20230053729A (ko) | 2019-10-31 | 2023-04-21 | 구미아이 가가쿠 고교 가부시키가이샤 | 제초제 및 그 중간체의 제조방법 |
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 |
| WO2000000031A1 (de) * | 1998-06-26 | 2000-01-06 | Novartis Pharma Ag. | Herbizides mittel |
| RU2237664C2 (ru) * | 1999-08-10 | 2004-10-10 | Кумиай Кемикал Индастри Ко., Лтд. | Изоксазолиновые производные и гербициды, содержащие их в качестве активных ингредиентов |
| DK1209973T3 (da) * | 1999-09-07 | 2004-06-21 | Syngenta Participations Ag | Herbicidt middel |
| 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 |
| DE60238194D1 (de) * | 2001-06-21 | 2010-12-16 | Kumiai Chemical Industry Co | Isoxazolinderivate und herbizide |
| 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 US US11/568,326 patent/US8404618B2/en active Active
- 2005-04-29 DE DE602005004283T patent/DE602005004283T2/de not_active Expired - Lifetime
- 2005-04-29 CA CA2829979A patent/CA2829979A1/en not_active Abandoned
- 2005-04-29 PL PL05741054T patent/PL1755397T3/pl unknown
- 2005-04-29 BR BRPI0510262-6A patent/BRPI0510262B1/pt not_active IP Right Cessation
- 2005-04-29 WO PCT/EP2005/004610 patent/WO2005104848A1/en not_active Ceased
- 2005-04-29 AU AU2005237241A patent/AU2005237241B2/en not_active Expired
- 2005-04-29 CA CA2563218A patent/CA2563218C/en not_active Expired - Fee Related
- 2005-04-29 AT AT05741054T patent/ATE383074T1/de not_active IP Right Cessation
- 2005-04-29 ES ES05741054T patent/ES2297709T3/es not_active Expired - Lifetime
-
2006
- 2006-10-09 ZA ZA200608416A patent/ZA200608416B/xx unknown
-
2011
- 2011-09-07 JP JP2011194494A patent/JP2012036191A/ja active Pending
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