http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H09268178-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01R33-28
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B57-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N24-08
filingDate 1996-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_68f5a3742f2b633f1aa9b61353914a21
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3431a0f568b9f1d9d8bc3ad4a3dde54d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7987415016855346576a932142ba61e7
publicationDate 1997-10-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H09268178-A
titleOfInvention Optically active 4,5-diphenyl-2-imidazolidinone derivative
abstract (57) [Summary] [Formula 1] (R 1 is an alkyl group, R 2 is an alkylene group, 1 is 0 or 1, and * is the position of the asymmetric carbon), and is an optically active 4,5-diphenyl-2-imidazolidinone derivative. A method for analyzing optical purity of amines having an asymmetric carbon used and a reagent for analysis. [Effect] By using this compound (1), the optical purity of amines having an asymmetric carbon can be accurately analyzed and determined by a simple operation.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8962848-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2014159418-A
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priorityDate 1996-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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