http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H0459759-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08F22-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G73-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08F22-36
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filingDate 1990-06-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_09f3011f57aedd39ebe9729db5b35296
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_13ea52b59e3fa7d47d9106a5d5d7ff8c
publicationDate 1992-02-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H0459759-A
titleOfInvention Flexible bisimide compound
abstract NEW MATERIAL:A flexible bisimide compound in which the terminal amino groups of an aromatic diamine expressed by the formula (X 1 to X 4 are H or 1-3C alkyl; R 1 and R 2 are H, CH 3 , C 2 H 5 , CF 3 or CCl 3 ; n is 1, 2 or 3) are imidated. n EXAMPLE: A flexible bismaleimide compound in which the terminal amino groups of 2,2-bis[4-(β-p-aminophenoxyethoxy)phenyl[propane are imidated. n USE: An intermediate capable of providing resins, useful as resins for fiber- reinforced composite materials, substrate resins for printed wiring boards, resins for heat-resistant molding materials, etc., and excellent in impact resistance and flexibility together with heat resistance due to the use of the aromatic diamine excellent in flexibility as the raw material. n PREPARATION: Aromatic diamines, excellent in the flexibility and expressed by the formula and an acid anhydride or an acid halide of maleic acid, nadic acid, etc., are subjected to imidating reaction according to a conventional method to afford the aforementioned flexible bisimide compound. n COPYRIGHT: (C)1992,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-WO2017209236-A1
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Total number of triples: 27.