http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H04209692-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ee1c19da359446fb5c4f0458a57b783d
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K9-02
filingDate 1990-12-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_250a9c2452a7ba6ed69834cd7eb96025
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8ac4cc38e9096b912f7821aaa4322a15
publicationDate 1992-07-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H04209692-A
titleOfInvention Photochromic material
abstract PURPOSE: To improve the durability in repeated photochrominism by coupling a specific indolenine derivative with a specific nitroso-hydroxy derivative. n CONSTITUTION: An indolenine derivative of formula IV is obtained by reacting an amine derivative of formula I (wherein R f is F or a polyfluoroalkyl; m≥2, ring A is an aromatic hydrocarbon ring that may be substituted by R f and other groups or an aromatic heterocyclic ring), a hydrazine derivative of formula II obtained by diazotizing and reducing the amino derivative and a ketone of formula III (wherein R 2 to R 4 are each H, a 1-25C hydrocarbon group, alkoxy, halogen, ester, cyano, nitro, ((thio)ether, etc.), followed by the Fischer indole reaction. Then, a nitroso-hydroxy derivative of formula VI is obtained by nitrosating a hydroxy compound of formula V (wherein ring B is identical to ring A). Subsequently, the indolenine derivative is made to react with a compound of formula VII (wherein X is SO 3 C 6 H 4 CH 3 ; R 1 is identical to R 2 ) and then with the nitroso-hydroxy derivative to obtain a photochromic material. n COPYRIGHT: (C)1992,JPO&Japio
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2015513597-A
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priorityDate 1990-12-03-04:00^^<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: 39.