Safener and pesticide is selected based on drug arylaminotriazoles 机翻标题: 暂无翻译,请尝试点击翻译按钮。

源语言标题
(JP2008506741) 選択​し​た​殺虫​剤​および​毒性​緩和​剤​に​基づく​殺虫​薬剤
公开号/公开日
JP2008506741 A 2008-03-06 [JP2008506741] / 2008-03-06
申请号/申请日
2007JP-0521875 / 2005-07-18
发明人
Fuitsushiya liner;Anderushiyu Borufuramu;Fungenberuku HEIKE;Teiereto Wolfgang;Birumusu Lothar;
申请人
BAYER CROPSCIENCE;
主分类号
IPC分类号
A01C-001/08A01M-001/20A01N-043/42A01N-043/54A01N-043/56A01N-043/80A01N-047/22A01N-053/08A01N-057/16A01P-007/04
摘要
(JP2008506741) Insecticidal compositions characterized by an effective amount of an active ingredient combination comprising (a) one or more compounds selected from the group of acetylcholinesterase inhibitors, sodium channel modulators, chitin biosynthesis inhibitors, juvenile hormone mimetics, chloride channel activators, ecdysone agonists, GABA-controlled chloride channel antagonists or acaricides, and (b) at least one crop plant tolerance promoter compound from the group of compounds specified in the description, which are used for controlling arthropods, and also methods of controlling arthropods through the treatment of plants and their seed with these compositions.  (From US2008293676 A1)
机翻摘要
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地址
代理人
代理机构
;
优先权号
2004DE-10035132 2004-07-20 2005WO-EP07792 2005-07-18
主权利要求
(JP2008506741)  1. An effective amount of a combination of active substances with a composition comprising, at least one acetylcholinesterase inhibitor (A) 1 [Azinphosmethyl, chlorpyrifos, diazinon, Dimethoate, Disulfoton, Ethion, Fenitrothion, Fenthion, Isoxathion, Malathion, Methidathion, Oxydemeton - methyl, Parathion, Parathion-methyl -, Fen To Art, folate, Phosalone, Hosumeto, Phoxim, Pirimiphos - methyl, Profenofos, Prothiofos, carbofuran, Triazophos, Chlorfenvinphos, Jikuroruhosu, Dicrotophos, Mevinphos, Monocrotophos, Phosphamidon, acephate, Metaamidohosu, Trichlorfon, carbaryl, Formetanate, Formetanate hydrochloride, methiocarb, Methomyl, oxamyl, Pirimicarb, Propoxur, from a series of thiodicarb. ] And/or at least one Sodium channel modulators (B) 1 [a group, cypermethrin α -, β - cyfluthrin, cyhalothrin, cypermethrin, deltamethrin, Esfenvalerate, etofenprox, fenpropathrin, fenvalerate, fenvalerate, λ - cyhalothrin, permethrin, esfenvalerate τ -, Tralomethrin, ζ - cypermethrin, Indoxacarb, from the series acrinathrin. ] 1 And/or at least one of the chitin biosynthesis inhibitor (C) [diflubenzuron, flucycloxuron, lufenuron, teflubenzuron, Triflumuron, from a series of cyromazine. ] And/or a juvenile hormone mimic (D) [Fenoxycarb, Diofenolan, from a series of pyriproxyfen. ] And/or at least one activating agent is 1 (E) chloride channels [abamectin, ivermectin, emamectin, milbemectin commute from. ] 1 And/or at least one ecdysone agonist/disruptor (F) [Methoxyfenozide, Tebufenozide from commute. ] 1 And/or at least one GABA (g) inhibiting ntsoidipine chloride channels [Endosulfan, gamma - HCH, from a series of fipronil. ] And/or at least one of the fungicides 1 (H) [etoxazole, Tebufenpyrad, Pyrimidifen, Dicofol, Toriaraten, Tetradifon, Propargite, Hexythiazox, Bromopropylate, - 1, 4-2 - -3 - (acetyloxy) commute Naphthalenedione from dodecyl. ] 1 And/or at least one biological compound and (I) [Amitraz, pymetrozine, Azadirachtin, spp.(Trichogramma spp.) Toriko Grandma, (Verticiliium lecanii) Bell lethal potassium Les crab Lee, buprofezin, Kinomechioneto, Thiocyclam hydrogen oxalate, Toriazamato, Thuringiensin, alphacy, diafenthiuron, from a series of spinosad. ] And less than or equal to 1 and at least one compound from the group consisting of a compound promoting tolerance of the crop, -4 - -1-4 - [4, 5] oxa - dichloroacetyl-azaspiro decane (AD-67, MON-4660), -6-3, 3, 8a - 1 - [1 .2 - a] Dichloro-acetyl-hexahydro Trimethyl pyrrolo-pyrimidine (2H) - on (Jishikuronon, BAS-145138), -3 - - dihydro - 4 - - methyl - - 3, 4 --dichloroacetyl - 2H-1, 4 (Benoxacor) benzoxazine, 5 - methylhexyl -8 - chloroquinoline Oxy-acetate 1 - (herbicidal composition - Populations .S. Cloquintocet EP-A-86750 -, with European Patent publication EP-A-94349, with European Patent publication EP-A-191736, European Patent Publication and related compounds of EP-A-492366 see.), 3 - (2 - - Chlorobenzyl) (-1 - - methyl - 1 - - phenylethyl) urea -1 - (Kumiruuron), α - (Cyano methoxyiminomethyl) phenylacetonitrile (Cyometrinil), 2, 4 - dichlorophenoxy acetic acid (2, 4-D), 4 - (2, 4 - dichlorophenoxy) butyric acid (2, 4-DB), -3 - (-1 - - methyl - 1 - - phenylethyl) 1 - (4 - - methylphenyl) urea ((daimuron) Daimuron, Daimuron (dymron)), -2 - - dichloro - 3, 6 - - methoxybenzoic acid (Dicamba), -1 - - methylacridan - -1 - - methyl Phenyl ethyl piperidine S-1 - (Dimepiperate), 2, 2 - - dichloro -N- (-2 - - oxo-ethyl 2 - (2 - Propenylamino) ) -N- (2 - propenyl) acetamide (DKA-24), 2, 2 - - dichloro - N, -2 - - di (Dichlormid) N- propenylacetamide, 4, 6 - -2 - - Dichloro - (Fenclorim) pyrimidines, -5 - (2, 4 - - dichlorophenyl) ethyl 1 - - trichloromethyl - -3 - - 1H-1, 2, 4 melt.These triazole (- ethyl - Fenchlorazole EP-A-174562 .S..S. published EP-A-346620 and association of the patent publication in reference compounds.), -5 - -4-2 - Trifluoromethyl thiazole melt.These Cidex (Fururazoru) phenylmethyl, 4 - - α - (1, 3 - - dioxolan - -2 - - ylmethoxy) -N- Trifluoro acetophenone oxime Cidex (Furukusofenimu), - 2, 2 - (2 - furanyl) -5 --dichloroacetyl Dimethyl oxazolidine 3 - (Furilazole, MON-13900), -3 - - diphenyl - - 5, 5 - - dihydro - 4, 5 --ethyl isoxazole (- ethyl - dispersibilization Isoxadifen in WO-A-95/07897 see related compounds.), -2 - (Ethoxycarbonyl) ethyl 3, 6 - - dichloro - 1 - (Rakuchijikuroru) methoxybenzoate, (4 - - chloro -o- tolyloxy) acetic acid (MCPA), 2 - (4 - - chloro -o- tolyloxy) propionic acid (Mecoprop), -5 - - dihydro - 1 - (2, 4 - - dichlorophenyl) methyl - - 4, 5 - - diethyl - - 1H --pyrazol - - 3, 5 - dicarboxylate ((mefenpyr-diethyl) - Mefenpyr-diethyl dispersibilization and related compounds in WO-A-91/07874 see.), - 1, 3 - - Dioxolan - 2 - - chloromethyl methyl (MG-191) -2 -, 2 - - propenyl -4 - - oxa - -4 - azaspiro [4. 5] decan - -1 - (MG-838) Calvo dithioates, naphthalic acid anhydride 1, 8 -, α - (-2 - - dioxolan - 1, 3 - Il methoxyiminomethyl) phenylacetonitrile (Oxabetrinil), 2, 2 - (-2 - - dioxolan - 1, 3 - - ylmethyl) -N- dichloro (2 - - propenyl) -N- acetamido (PPG-1292), 3 - (R-28725) Dimethyl oxazolidine - 2, 2 - dichloroacetyl, dichloroacetyl-- 2, 2 3 -, 5 - Trimethyl oxazolidine (R-29148), 4 - (4 - - chloro -o- tolyl) butyric acid, 4 - (4 - - chlorophenoxy) butyric acid, diphenylmethoxy acetic acid, Methyl diphenyl methoxy acetate, Ethyl acetate diphenylmethoxy, - 1H - (2 - - chlorophenyl) pyrazol - 1 - - methyl-phenyl -5 - -3 - carboxylate, ethyl -3-1 - - 1H - -5 - (2, 4 - - dichlorophenyl) methyl pyrazole carboxylate, ethyl -3 - -5-1 - - 1H - (2, 4 - - dichlorophenyl) pyrazole isopropyl carboxylate, ethyl (1, 1 - - dimethylethyl) (2, 4 - - dichlorophenyl) 1 - - 1H - -5 - -3 - pyrazole melt.These, pyrazol - -5 - (2, 4 - - dichlorophenyl) ethyl - 1H - phenyl 1 - -3 - carboxylate (published European Patent EP EP-A-269806 and related compounds of EP-A-333131 see.), -3 - (2, 4 - Dichlorobenzyl) -2 - isoxaaolin 5 - ethyl carboxylate, ethyl -2 - phenyl 5 - -3 - isoxaaolin carboxylate, ethyl -2 - phenyl 5 - -3 - -5 - (4 - - fluorophenyl) carboxylate isoxaaolin (International Publication in WO-A-91/08202 see related compounds.), -1 - - Dimethylbut-l 1, 3-5 - -8 - chloroquinoline Oxy-acetate, 5-4 - -8 - chloroquinoline Oxy-acetate Allyl oxy butyl, l 1-5 - -2 - -8 - chloroquinoline Oxy-acetate Allyloxy property, 5 - methyl -8 - Oxy-acetate Chloroquinoxaline, 5 - ethyl -8 - chloroquinoline Oxy-acetate, 5 - allyl Oxy-acetate Chloroquinoxaline -8 -, l 2-5 - -1 - -8 - chloroquinoline Oxy-acetate Okisopuropa, -8 - chloroquinoline Oxy malonate or diethyl 5 -, -8-5 - diallyl Chloroquinoxaline Oxy malonate, Oxy malonate or diethyl -8 - chloroquinoline 5 - (EP-A-582198 in European Patent Publication see related compounds.), -4 - Yl acetate Carboxyanhydride cyclo Man 4 - (AC-304415, European Patent Publication EP-A-613618 see.), 4 - - Chlorophenoxy acetic acid, 3, 3' -4 - - Dimethyl-benzophenone, -4 - - bromo - 1 - Chloromethyl sulfonylbenzene, 1 - [4 - (N-2 - Methoxybenzoyl ylsulfamoyl) phenyl] -3 - methyl (N - -4 - (2 - - methoxybenzoyl) [(ethylaminocarbonyl) amino] benzenesulfonamide also known as.), 1 - [4 - (N-2 - Methoxybenzoyl ylsulfamoyl) phenyl] - 3, 3 - dimethylurea, 1 - [4 - (N-4, 5 - Dimethylbenzo ylsulfamoyl) phenyl] methyl -3 -, -3 [4 - (N - Naphthylsulfinyl sulfamoylbutyl) phenyl] 1 -, 3 - Dimethylurea, -4 - (2 - methoxy -5 - methylbenzoyl) N- (Cyclopropylaminocarbonyl) benzenesulfonamide, represented by the general formula (IIa)   (IIb) or the general formula  (IIc) or the general formula  of the compounds of the general formula 1 as defined by one [in the formula, m represents a number of from 5 0 the, A1 dyadic shown below 1 represents one of the group consisting of heterocyclic,  n5 represent a number from 0 the, A2 is optionally C1 -C4 -alkyl, C1 -C4 -alkoxy carbonyl - and or -C1 -C4 -- alkenyloxy which is substituted by a carbonyl, having 1 to 2 carbon atoms or represents alkanediyl, R8 is hydroxyl, mercapto, amino, C1 -C6 -alkoxy, C1 -C6 -alkylthio, C1 -C6 -represents alkylamino or di (C1 -C4 -alkyl) amino, R9 is hydroxyl, mercapto, amino, C1 -C7 -alkoxy, C1 -C6 -alkenyloxy, C1 -C6 -alkenyloxy -C1 -C4 -alkoxy, C1 -C6 -alkylthio, C1 -C6 -represents alkylamino or di (C1 -C4 -alkyl) amino, R10 is in each case optionally fluorine, chlorine and/or bromine-substituted C1 -C4 -alkyl, R11 hydrogen, in each case optionally, fluorine, chlorine and/or bromine-substituted C1 -C6 -alkyl, C2 -C6 -alkenyl or C2 -C6 -alkynyl, C1 -C4 -alkoxy -C1 -C4 -alkyl, dioxolanyl -C1 -C4 -alkyl, furyl, furyl -C1 -C4 -alkyl, thienyl, thiazolyl, piperidinyl, or optionally fluorine, chlorine and/or bromine or C1 -C4 -represents a phenyl group substituted with alkyl, R12 hydrogen, in each case optionally fluorine, chlorine and/or bromine-substituted C1 -C6 -alkyl, C2 -C6 -alkenyl or C2 -C6 -alkynyl, C1 -C4 -alkOXy -C1 -C4 -alkyl, dioxolanyl -C1 -C4 -alkyl, furyl, furyl -C1 -C4 -alkyl, thienyl, thiazolyl, piperidinyl, or optionally fluorine, chlorine and/or bromine or C1 -C4 -represents a phenyl group substituted with alkyl, R11 and R12 together, in any of these cases optionally C1 -C4 -alkyl, phenyl, furyl, fused with a benzene ring or by means of, together with the atoms to which they are attached to the 6 or 5 C Otis 2 to form a ring carbon is substituted by three substituents C3 -C6 -alkanediyl or C2 -C5 -represent Oxa alkanediyl, R13 is hydrogen, cyano, or represents halogen, in each case optionally fluorine, chlorine and/or bromine-substituted C1 -C4 -alkyl, C3 -C6 -represents cycloalkyl or phenyl, R14 is hydrogen, optionally hydroxyl -, cyano -, with a halogen or an C1 -C4 -alkoxy substituted C1 -C6 -alkyl, C3 -C6 -represents cycloalkyl or tri (C1 -C4 -alkyl) silyl, R15 is hydrogen, cyano, or represents halogen, in each case optionally fluorine, chlorine and/or bromine-substituted C1 -C4 -alkyl, C3 -C6 -represents cycloalkyl or phenyl, X1 is nitro, cyano, halogen, C1 -C4 -alkyl, C1 -C4 -haloalkylinclude, C1 -C4 -alkoxy or C1 -C4 -represents haloalkoxy, X2 is hydrogen, cyano, nitro, halogen, C1 -C4 -alkyl, C1 -C4 -haloalkylinclude, C1 -C4 -alkoxy or C1 -C4 -represents haloalkoxy, X3 is hydrogen, cyano, nitro, halogen, C1 -C4 -alkyl, C1 -C4 -haloalkylinclude, C1 -C4 -alkoxy or C1 -C4 -FWRl haloalkoxy. ], And/or the formula (IId)  or the formula (IIe)  compound defined by the structure of the general formula [in the formula, r and s represent a number from 0 is 5, R16 is hydrogen or a Cl C1 -C4 -alkyl, R17 is hydrogen or a Cl C1 -C4 -alkyl, R18 hydrogen, in each case optionally cyano -, halogen or C1 -C4 -alkoxy substituted C1 -C6 -alkyl, C1 -C6 -alkoxy, C1 -C6 -alkylthio, C1 -C6 -(C1 -C4 -alkyl) amino or di-alkylamino, cyano or in each case optionally, halogen or C1 -C4 -alkyl substituted C3 -C6 -Cycloalkjd, C3 -C6 -cycloalkyloxy, C3 -C6 -cycloalkylthio or C3 -C6 -represents cycloalkylamino, R19 is hydrogen, optionally cyano -, hydroxyl, halogen or C1 -C4 -alkoxy substituted C1 -C6 -alkyl, cyano or optionally in each case be substituted by a halogen C3 -C6 -alkenyl or C3 -C6 -alkynyl, or optionally cyano, with a halogen or an C1 -C4 -alkyl substituted C3 -C6 -represent cycloalkyl, R20 is hydrogen, optionally cyano -, hydroxyl, halogen or C1 -C4 -alkoxy substituted C1 -C6 -alkyl, in each case optionally cyano - or halogen-substituted C3 -C6 -alkenyl or C3 -C6 -alkynyl, optionally cyano -, halogen or C1 -C4 -alkyl substituted C3 -C6 -cycloalkyl, or optionally nitro -, cyano -, halogen, C1 -C4 -alkyl, C1 -C4 -haloalkyl, C1 -C4 -alkoxy or C1 -C4 -haloalkoxy or represents optionally substituted phenyl, R19 together with in either case optionally C1 -C4 -alkyl substituted C2 -C6 -alkanediyl or C2 -C5 -Oxa alkanediyl represents, X4 is nitro, cyano, carboxyl, carbamoyl, formyl, sulfamoyl, hydroxyl, amino, halogen, C1 -C4 -alkyl, C1 -C4 -haloalkylinclude, C1 -C4 -alkoxy or C1 -C4 -represents haloalkoxy, and X5 is nitro, cyano, carboxyl, carbamoyl, formyl, sulfamoyl, hydroxyl, amino, halogen, C1 -C4 -alkyl, C1 -C4 -haloalkylinclude, C1 -C4 -alkoxy or C1 -C4 -FWRl haloalkoxy. ] Composition.  2. The primary active component, herbicidal composition Cloquintocet -, ethyl - Fenchlorazole, Isoxadifen - ethyl, diethyl Mefenpyr -, Furilazole, Fenclorim, Cumyluron, Daimuron, Dimepiperate, compound IIe-5, 1 of at least one of the compounds IIe-11 resistant crops contained as promoting compound characterized in that the composition according to claim 1.  3. For controlling arthropod, the composition according to claim 1.  4. A composition according to claim 1 arthropods and/or their habitat and allowing to act, arthropods.  5. For the protection of seeds from the arthropod, the composition according to claim 1.  6. Is treated with a composition according to claim 1 seed characterized in that, of the seed from trypa patternNum method.  7. Which is treated with a composition according to claim 1 and seeds.
法律状态
(JP2008506741) LEGAL DETAILS FOR JP2008506741  Actual or expected expiration date=2011-09-06    Legal state=DEAD    Status=REVOKED     Event publication date=2005-07-18  Event code=JP/APP  Event indicator=Pos  Event type=Examination events  Application details  Application country=JP JP2007521875  Application date=2005-07-18  Standardized application number=2007JP-0521875     Event publication date=2008-03-06  Event code=JP/A  Event indicator=Pos  Event type=Examination events  Published application  Publication country=JP  Publication number=JP2008506741  Publication stage Code=A  Publication date=2008-03-06  Standardized publication number=JP2008506741     Event publication date=2008-07-02  Event code=JP/A621  Event indicator=Pos  Event type=Examination events  Written request for application examination  Effective date of the event=2008-07-01  JAPANESE INTERMEDIATE CODE: A621     Event publication date=2011-09-07  Event code=JP/A02  Event indicator=Neg  Event type=Event indicating Not In Force  Decision of refusal  Effective date of the event=2011-09-06  JAPANESE INTERMEDIATE CODE: A02
专利类型码
A
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