http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S6061586-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24aca9ded2638ea793d05360dde7a4a0
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-17
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N57-12
filingDate 1983-09-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bcca870def474c3f01cc3c64bfc8b379
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_88ad11b1db2fd6ea03ace13c8b982263
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5eaa9e36e325e002b7e6a75eeef45bd0
publicationDate 1985-04-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S6061586-A
titleOfInvention Dithiolphosphoric acid ester, its production and soil vermin controlling agent containing said ester as active component
abstract NEW MATERIAL:The compound of formula I (R is iso-propyl or iso-butyl). n EXAMPLE: O-Methyl S-iso-propyl S-iso-butyl phosphorodithiolate. n USE: Agent for controlling soil vermin effective to soil vermin of paddy field, plowed land, orchard, etc. (e.g. western corn root worm). n PREPARATION: The compound of formula I can be produced by reacting 1 equivalent of the halogenated thiophosphoric acid derivative of formula II (X is halogen) with 1W5 equivalent of the alkyl mercaptan of formula R'SH (when R=iso-propyl, R' is iso-butyl and when R=iso-butyl, R' is iso-butyl or iso-propyl). The reaction is carried out in a solvent such as acetone, methyl ethyl ketone, etc. or in the absence of solvent, and in the presence of 1.0W1.5 equivalent of a dehydrohalogenation agent and a phase-transfer catalyst of a copper catalyst. n COPYRIGHT: (C)1985,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-100388976-C
priorityDate 1983-09-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 22.