Improvement on insecticide 机翻标题: 暂无翻译,请尝试点击翻译按钮。

源语言标题
(JP1992350) 殺​中​剤​に関する​改良
公开号/公开日
JPS6147436 A 1986-03-07 [JP61047436]JPH0717558 B2 1995-03-01 [JP95017558]JP1992350 C 1995-11-22 [JP1992350] / 1986-03-071995-03-011995-11-22
申请号/申请日
1985JP-0169655 / 1985-07-30
发明人
MAIKERU ERIOTSUTO;NOOMAN FURANKU JIEINZU;BUPINDAA POORU SHINGU KIYANBEI;
申请人
NATIONAL RESEARCH DEVELOPMENT;
主分类号
IPC分类号
A01N-035/02A01N-035/04A01N-053/00A01N-053/02A01N-053/04C07C-045/00C07C-045/45C07C-049/577C07C-049/80C07C-049/813C07C-067/00C07C-253/00C07C-255/40C07D-317/54C07D-333/32
摘要
(JP1992350) Pesticidal compounds of formula I, the preparation of such compounds, intermediates for use in their preparation compositions containing such compounds and the use of such compounds and compositions to prevent or control pest infestation.  Compounds of I have the following formula: I RACOCHDRB in which formula: RA represents a group ArCR1R2- in which Ar represents a phenyl or naphthyl group optionally substituted by one or more halogen, haloalkoxy, methylenedioxy or C1-C6 alkyl groups; R1 representing methyl, ethyl, isopropyl or cycloalkyl; R2 representing hydrogenn or methyl; or R1 and R2 together with the carbon to which they are attached representing join@@y a cycloalkyl group optionally carrying one or more halogen substituents; or RA represents the residue of a pyrethroidal acid RACO2H the 5-benzyl-3-furylmethyl ester of which is significantly insecticidal; RB represents the residue of an alcohol RBCHDOH in which D is hydrogen or cyano and of which the [IR, cis] 2,2-dimethyl-3-(2,2-dibromovinyl)cyclopropane carboxylic ester is significantly insecticidal, provided that then the alcohol is of formula II: <CHEM> RA is other than the residue of chrysanthemic acid.  (From EP0171249 A2)
机翻摘要
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地址
代理人
代理机构
;
优先权号
1984GB-0019339 1984-07-30
主权利要求
(JP95017558)   1. Formula I: R [A] COCHQR [B] I [In formula, R [as for A] acid below: Chrysanthemum acid and pyrethrin acid (pyrethri c acid) Dimethyl cyclopropane carboxylic acid, tetra- Methyl cyclopropane carboxylic acid, 2,2 - dimethyl - 3 - (2,2 - [jiburomobiniru]) cyclopropane carbon Acid, 2,2 - dimethyl - 3- (2,2 - [jikurorobiniru]) [shiku] [ropuropankarubon] , 2,2 - dimethyl - 3- (1,2,2,2 - [tetoraburomoechiru]) cyclopropane carboxylic acid, 2, 2 - Dimethyl - 3- (1,2 - [jiburomo] - 2,2 - [jikuroroe] Chill) cyclopropane carboxylic acid, 2,2 - dimethyl - 3 - (2 - [kuroro] - 3,3,3 - [torihuruoropuropeniru]) [shi] Clo propane carboxylic acid, or 2,2 - dimethyl - 3- (Tetrahydrofolic - 2 - oxo - [chieni] - 3 - [iridenme] Chill) acid residue of cyclopropane carboxylic acid; R [B] as for CHQ 3 - phenoxy benzyl, 4 - phenoxy Venn Gill, ***.alpha.-shiano - 3 - phenoxy benzyl, 4 - full [oro] - 3 - phenoxy benzyl, ***.alpha.-shiano - 4 - full [oro] - 3 - phenoxy benzyl, 5 - benzyl - 3 - [hu] Rill methyl, 3 - benzyl benzyl, 4 - benzyl Venn Gill, 3 - phenyl - 2 - methyl benzyl or 3 - [hu] [eniru] - 2 - [aruko] which is [kurorobenjiruarukoru] [ru] R [B] the residue of CHQOH is displayed] with the chemical compound which is displayed.  2. Formula: R [A] COX [In formula, R [as for A] acid below: Chrysanthemum acid and pyrethrin acid (pyrethri c acid) Dimethyl cyclopropane carboxylic acid, tetra- Methyl cyclopropane carboxylic acid, 2,2 - dimethyl - 3 - (2,2 - [jiburomobiniru]) cyclopropane carbon Acid, 2,2 - dimethyl - 3- (2,2 - [jikurorobiniru]) [shiku] [ropuropankarubon] , 2,2 - dimethyl - 3- (1,2,2,2 - [tetoraburomoechiru]) cyclopropane carboxylic acid, 2, 2 - Dimethyl - 3- (1,2 - [jiburomo] - 2,2 - [jikuroroe] Chill) cyclopropane carboxylic acid, 2,2 - dimethyl - 3 - (2 - [kuroro] - 3,3,3 - [torihuruoropuropeniru]) [shi] Clo propane carboxylic acid, or 2,2 - dimethyl - 3- (Tetrahydrofolic - 2 - oxo - [chieni] - 3 - [iridenme] Chill) acid residue of cyclopropane carboxylic acid;  As for X halogen Or substitution amide is displayed] with the chemical compound which is displayed and, Formula: R [B] CHQM [In formula, R [B] as for CHQ 3 - phenoxy benzyl, 4 - [hueno] [kishibenjiru] and ***.alpha.-shiano - 3 - phenoxy benzyl, 4 - Fluoro - 3 - phenoxy benzyl, ***.alpha.-shiano - 4 - Fluoro - 3 - phenoxy benzyl, 5 - benzyl - 3 - Frill methyl, 3 - benzyl benzyl, 4 - Venn Gill benzyl, 3 - phenyl - 2 - methyl benzyl and 3 - Phenyl - 2 - it is [kurorobenjiruarukoru] Alcohol R [B] the residue of CHQOH;  As for M metal or metal content part You display] with it reacts with the organic metal test medicine which is displayed densely That the formula I which is featured: R [A] COCHQR [B] I [In formula, R [A] and R [B] CHQ is displayed with the same meaning as the description above] Manufacturing method of chemical compound.  3. Formula I: R [A] COCHQR [B] I [In formula, R [as for A] acid below: Chrysanthemum acid and pyrethrin acid (pyrethri c acid) Dimethyl cyclopropane carboxylic acid, Tet lame Chill cyclopropane carboxylic acid, 2,2 - dimethyl - 3- (2,2 - [jiburomobiniru]) cyclopropane carboxylic acid, 2,2 - Dimethyl - 3- (2,2 - [jikurorobiniru]) [shikuropu] [ropankarubon] , 2,2 - dimethyl - 3- (1,2,2,2 - [te] [toraburomoechiru]) cyclopropane carboxylic acid, 2,2- Dimethyl - 3- (1,2 - [jiburomo] - 2,2 - [jikuroroechi] [ru]) cyclopropane carboxylic acid, 2,2 - dimethyl - 3- (2 - [kuroro] - 3,3,3 - [torihuruoropuropeniru]) [shiku] [ropuropankarubon] , or 2,2 - dimethyl - 3- (Tetrahydrofolic - 2 - oxo - [chieni] - 3 - [iridenme] Chill) acid residue of cyclopropane carboxylic acid; R [B] as for CHQ 3 - phenoxy benzyl, 4 - phenoxy Venn Gill, ***.alpha.-shiano - 3 - phenoxy benzyl, 4 - full [oro] - 3 - phenoxy benzyl, ***.alpha.-shiano - 4 - full [oro] - 3 - phenoxy benzyl, 5 - benzyl - 3 - [hu] Rill methyl, 3 - benzyl benzyl, 4 - benzyl Venn Gill, 3 - phenyl - 2 - methyl benzyl or 3 - [hu] [eniru] - 2 - [aruko] which is [kurorobenjiruarukoru] [ru] R [B] the chemical compound which is displayed with the residue of CHQOH] the inactive carrier [ma] It is diluent The insecticide which is contained together.  4. The environment which is easy to have an influence on spreading of the noxious insect or the noxious insect Formula I:  R [A] COCHQR [B] I  [In formula, R [as for A] acid below: Chrysanthemum acid and pyrethrin acid (pyrethri c acid) Dimethyl cyclopropane carboxylic acid, tetra- Methyl cyclopropane carboxylic acid, 2,2 - dimethyl - 3 - (2,2 - [jiburomobiniru]) cyclopropane carbon Acid, 2,2 - dimethyl - 3- (2,2 - [jikurorobiniru]) [shiku] [ropuropankarubon] , 2,2 - dimethyl - 3- (1,2,2,2 - [tetoraburomoechiru]) cyclopropane carboxylic acid, 2, 2 - Dimethyl - 3- (1,2 - [jiburomo] - 2,2 - [jikuroroe] Chill) cyclopropane carboxylic acid, 2,2 - dimethyl - 3 - (2 - [kuroro] - 3,3,3 - [torihuruoropuropeniru]) [shi] Clo propane carboxylic acid, or 2,2 - dimethyl - 3- (Tetrahydrofolic - 2 - oxo - [chieni] - 3 - [iridenme] Chill) acid residue of cyclopropane carboxylic acid;  And R [B] as for CHQ 3 - phenoxy benzyl, 4 - [huenoki] [shibenjiru] and ***.alpha.-shiano - 3 - phenoxy benzyl, 4 - Fluoro - 3 - phenoxy benzyl, ***.alpha.-shiano - 4 - Fluoro - 3 - phenoxy benzyl, 5 - benzyl - 3 - Frill methyl, 3 - benzyl benzyl, 4 - [benji] [rubenjiru], 3 - phenyl - 2 - methyl benzyl or 3 - Phenyl - 2 - [a] which is [kurorobenjiruarukoru] [rukoru] R [B] the effective quantity of the chemical compound which is displayed with the residue of CHQOH] So the method which prevents spreading of the noxious insect which features that it processes Law.
法律状态
(JP1992350) LEGAL DETAILS FOR JPS6147436  Actual or expected expiration date=2005-07-30    Legal state=DEAD    Status=EXPIRED     Event publication date=1985-07-30  Event code=JP/APP  Event indicator=Pos  Event type=Examination events  Application details  Application country=JP JP16965585  Application date=1985-07-30  Standardized application number=1985JP-0169655     Event publication date=1986-03-07  Event code=JP/A  Event indicator=Pos  Event type=Examination events  Published application  Publication country=JP  Publication number=JPS6147436  Publication stage Code=A  Publication date=1986-03-07  Standardized publication number=JP61047436     Event publication date=1995-03-01  Event code=JP/B2  Event indicator=Pos  Event type=Event indicating In Force  Published granted patent (Second level)  from 01-03-1996 onwards (Published examined patent application (Second level) 1971-1996)  Publication country=JP  Publication number=JPH0717558  Publication stage Code=B2  Publication date=1995-03-01  Standardized publication number=JP95017558     Event publication date=1995-11-22  Event code=JP/C  Event indicator=Pos  Event type=Event indicating In Force  Granted patent from 1000001 onwards  Publication country=JP  Publication number=JP1992350  Publication stage Code=C  Publication date=1995-11-22  Standardized publication number=JP1992350     Event publication date=2005-07-30  Event code=JP/EEDX  Event indicator=Neg  Event type=Event indicating Not In Force  Patent has expired
专利类型码
AB2C
国别省市代码
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