http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102639476-B

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2603-24
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C39-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C39-15
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G8-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C39-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C37-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C39-15
filingDate 2010-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-08-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2015-08-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102639476-B
titleOfInvention Anthracene derivant, the compound using it, composition, cured article and manufacture method thereof
abstract The object of this invention is to provide and a kind ofly have such as high carbon density, high-melting-point, high refractive index concurrently and there is the distinctive characteristic of the anthracenes such as fluorescence under uviolizing and result from the multifarious anthracene derivant of reaction of bis-phenol structure and manufacture method thereof.The present invention is the anthracene derivant (in general formula (I), X and Y represents hydroxyaryl independently of one another) that following general formula (1) represents.Described X and Y is preferably hydroxy phenyl.In addition, described anthracene derivant can be manufactured by the method comprising following operation, and described operation is under the existence of non-reacted Aqueous organic solvent and acid catalyst, phenols and 9-anthraldehyde are reacted.
priorityDate 2009-10-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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