http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5068230-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N57-28
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filingDate 1989-10-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1991-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b03b5952c1c49074e232597b7d66b669
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_abb5ffae7eb733d28a80a67ce566e27b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8887d0f8d719577da85894683560a1a9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7ae790425749310c69500142e3ec0f51
publicationDate 1991-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5068230-A
titleOfInvention N-(((alkoxy(alkylthio)phosphinyl)amino)carbonyl)-aminoalkanoate ester insecticides
abstract Ester and amide derivatives of N-(((alkoxy-(alkylthio)phosphinyl)amino)carbonyl)amino)alkanecarboxylic acids of the formula: ##STR1## (wherein R 2 represents an alkyl group containing a carboxylic acid ester or amide moiety) were prepared by the reaction of O,S-dialkyl phosphoroisocyanatidothioates and ester and amide derivatives of naturally occurring and synthetic aminoacids and were found to be effective plant systemic and contact insecticides. Ethyl N-(((methoxy(methylthio)phosphinyl)amino)-carbonyl)methioninate, for example, were prepared from O,S-dimethyl phosphoroisocyanatidothioate and ethyl methioninate and found to control aster leafhoppers when applied to rice plants.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9300089-A1
priorityDate 1989-10-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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