http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S62242686-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_129e393582e6bdf4029baf2206522f45
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K9-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D491-08
filingDate 1986-04-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3fa184eae0d3d56f8b2a130ec6d626e0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1a64f2a0a4ce22bf24bf7edb9351489f
publicationDate 1987-10-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S62242686-A
titleOfInvention Novel spiropyran compound
abstract NEW MATERIAL:A compound of formula I (R 1 WR 4 are H or 1W6C alkyl; R 5 and R 6 are OH, NH 2 , organic-substituted amino, 1W6C alkoxy, 7W11C aralkoxy, 6W10C aryloxy, halogen, CN, etc.; l and m are 0W4; n is 1W6). n EXAMPLE: 1'-Carbamoylmethyl-3', 3'-dimethyl-6-nitrospiro [2H-1-benzopyran-2,2'- indoline]. n USE: A photochromic material for printing and optical instrument, etc. It has high rate of color development and extinction and excellent acid resistance and is stable even in an organopolysiloxane system. It is added to a resin at an amount of preferably 0.01W10wt%. n PREPARATION: The objective compound can be produced e.g. by reacting a compound of formula II (e.g. 1-carbamoylmethyl-2-methylene-3,3-dimethylindoline) with a compound of formula III (e.g. 5-nitrosalicylaldehyde) in a solvent such as ethanol. n COPYRIGHT: (C)1987,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9420502-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2011524428-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102036994-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2009141237-A1
priorityDate 1986-04-16-04:00^^<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: 27.