http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S5988461-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6918131ce5bf2cf19b25c88e02b92fc6
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-86
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-86
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00
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filingDate 1982-11-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c03871194380dbbe0260019a9b222902
publicationDate 1984-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S5988461-A
titleOfInvention Carbamate insecticide
abstract NEW MATERIAL:The compound of formula I [Ar is group of formula II or formula III; R 1 is -X-COO-R 3 (X is 1W6C alkylene; R 3 is 1W8C alkyl) or -Y-CN (Y=X); R 2 is -(CH 2 ) n -O-R 4 (R 4 is 1W5C alkyl, 3W6C cycloalkyl, phenyl or benzyl; n is 2W5)]. n EXAMPLE: 2,3-Dihydro-2,2-dimethylbenzofuran-7-yl N-(N-methoxyethyl-N-ethoxycarbonylmethylaminosulfenyl) N-methyl carbamate. n USE: Insecticide having extreme insecticidal and controlling effects to the vermin of Hemiptera, Lepidoptera, etc., and agricultural, forestry or hygienic vermin such as mites. n PROCESS: The compound of formula I can be prepared by reacting the carbamate derivative of formula IV with the aminosulfenyl chloride derivative of formula V. n COPYRIGHT: (C)1984,JPO&Japio
priorityDate 1982-11-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 24.