http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S63267783-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_73ebc284a55d5daf0e209d6186c9e65c
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K9-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D498-10
filingDate 1987-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f3654464d87ad2940eaf9d550a93d0ab
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ceea8f8a2eda482c37e98fd4b39a7054
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ff113f1e69785ec9e799d529e3e37387
publicationDate 1988-11-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S63267783-A
titleOfInvention Photochromic compound
abstract NEW MATERIAL:The compound of formula (R 1 is substituent having saturated hydrocarbon ring as a principal skeleton; R 2 WR 5 and R 9 WR 14 are lower alkyl, nitro, etc.; R 6 and R 7 are H, benzyl, etc.; R 8 is H, lower alkyl, etc.; n is integer of 1W30). n EXAMPLE: 1-Cyclohexylmethyl-3,3,4,6-tetramethylspiro[indolino-2,3'-(9'-methoxyna phtho)[2,1-b][1,4]-oxazine]. n USE: A photochromic material having high molar extinction coefficient and excel lent durability and temperature characteristics, etc., of color-development. n PREPARATION: The exemplified compound can be produced e.g. by reacting 2,3,3,4,6-pentamethylindolenine with (bromomethyl)cyclohexane and reacting the resultant 1-cyclohexylmethyl-2,3,3,4,6-pentamethylindolenine bromine salt with 7-methoxy-1-nitroso-2-naphthol. n COPYRIGHT: (C)1988,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9216538-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5288592-A
priorityDate 1987-04-23-04:00^^<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: 29.