http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2041531-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_fd9859f29d348e8f3fd06f6088b1177d
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G02F1-3616
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G65-4012
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G02F1-361
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G65-40
filingDate 1991-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b981eb19514209f98807148105ae0177
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_596c822fd8b571e53b1ac389c1aca9ab
publicationDate 1991-12-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2041531-A1
titleOfInvention Aromatic polyethers containing azo groups
abstract Mo-3453 AROMATIC POLYETHERS CONTAINGING AZO GROUPS ABSTRACT OF THE DISCLOSURE A dihalobenzenoid compound is reacted with a dihydric phenol containing an azo group in the presence of a base, an organic solvent and an azeotrope former. Dihydric phenols which do not contain azo groups may also be included in the reactin mixture. This reaction is generally carried out at a temperature of from about 20 to about 250°C under an inert atmosphere. The polyether obtained is represented by the formula [-O-[E-O]z-E']x [O-E"-O-E'-]y in which E, E', E", x, y and z have the meaning specified herein. Mo-3453
priorityDate 1990-05-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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