http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S6330584-A

Outgoing Links

Predicate Object
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D265-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K9-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D498-10
filingDate 1986-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d347d0bdedf6a7384424ec5566574fb8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6721ed6d7d811147eea5aed866082c30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_90bc8b6e974fc9bef14d834ec2d846cd
publicationDate 1988-02-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S6330584-A
titleOfInvention Photochromic substance
abstract PURPOSE: To obtain a photochromic substance which has a high capacity of absorbing the light in a long-wavelength region and excellent resistance to repeated use, and gives a photochromic optical material having an excellent light controlling function, by using a specified spironaphthoxazine compound. n CONSTITUTION: A spironaphthoxazine compound of the formula (wherein R 1 is H, a halogen, cyano, a 1W6C alkyl or 1W6C alkoxy; R 2 is a substituted arylalkyl, a 1W6C alkyl, a 2W6C alkoxyalkyl, etc.) is used as a photochromic substance.A spironaphthoxazine compound of the formula is synthesized by reacting 2,6-dihydroxy-1,5-dinitrosonaphthalene with a corresponding indoline compound. A photochromic optical material having an excellent light controlling function can be obtained by incorporating this photochromic substance into a matrix comprising an optically transparent resin. n COPYRIGHT: (C)1988,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H04208289-A
priorityDate 1986-07-24-04:00^^<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.