http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H01211562-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-452
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G73-12
filingDate 1988-02-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ba7c24755cd214bd5efab172248c9df1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_73a5165336b5b70a9dacd6ae87567a2a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_232b77d695f8450d1d729cce0c06dc33
publicationDate 1989-08-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H01211562-A
titleOfInvention Novel bismaleimide and production thereof
abstract NEW MATERIAL:3,4-Bismaleimide diphenyl ether of the formula. n USE: A starting substance for bismaleimide resins. n PREPARATION: 3,4'-Diaminodiphenyl ether is mixed with 2 equivalent amount of maleic anhydride in an inert solvent such as diethyl ether to form amide- carboxylic acid, then the product is dehydrative cyclization to give the compound of the formula. The dehydrative cyclization is carried out by heating the amide-carboxylic acid 80W200°C or by using a condensation agent such as acetic acid at 10W80°C for 20minW8hr. When a condensation agent is used, a catalyst such as sodium acetate may be added, when needed. n COPYRIGHT: (C)1989,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5606061-A
priorityDate 1988-02-17-04:00^^<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.