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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_b19eaa8e535da4e4bceed99917a68153
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C227-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C229-60
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-65
filingDate 2004-01-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a1d21fdbd651ce22bedb06e4243ee9cd
publicationDate 2005-08-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2005213199-A
titleOfInvention Aromatic diamine and its hydrochloride, and method for synthesizing aromatic diamine, aromatic bisaminophenol and its hydrochloride
abstract PROBLEM TO BE SOLVED: To provide a novel aromatic diamine useful as a raw material for a condensation polymer having high heat resistance. An aromatic diamine represented by the general formula (1) and a hydrochloride thereof. [Chemical 1] [In the formula (1), Z represents a carboxyl group or an active ester group represented by the following general formula (2). The hydrogen atom on the benzene ring in the group represented by the formula (1) is at least one group selected from an alkyl group, an aromatic group, an ether group, a hydroxyl group, a fluorine atom and a trifluoromethyl group. It may be replaced. ] [Chemical 2] [In Formula (2), R shows an alkyl group, a pyridyl group, a quinolyl group, an aromatic group, or a benzotriazole group. The hydrogen atom in the alkyl group, pyridyl group, quinolyl group, aromatic group, and benzotriazole group may be substituted with at least one organic group. ]
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9520569-B2
priorityDate 2004-01-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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