http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H07224005-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-76
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-757
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-753
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G02F1-13
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K19-54
filingDate 1994-02-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_33701ea2b1d4bd8b0d2db8c81f4545a3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_37732221e6153c6f79f066413cb0747d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_60e931d6a0f2da1b84bf509ef9871eb0
publicationDate 1995-08-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H07224005-A
titleOfInvention Carboxylic acid ester compound and liquid crystal additive
abstract (57) [Summary] [Structure] The carboxylic acid ester compound of the present invention is represented by the following formula. R-A-COO-R 'In the formula, R represents an alkyl group having 1 to 20 carbon atoms, an alkoxy group, or an aryloxy group, A represents a tetrahydronaphthalene ring, and R'is the above R. They are different alkyl groups having 1 to 10 carbon atoms or hydrogen atoms. Further, in the carboxylic acid ester compound of the present invention, the tetrahydronaphthalene ring may have optical activity. The liquid crystal additive of the present invention is composed of the carboxylic acid ester compound as described above. [Effect] By mixing the carboxylic acid ester compound of the present invention with a liquid crystal compound for use, liquid crystal characteristics can be improved.
priorityDate 1994-02-10-04:00^^<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: 47.