http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H02104562-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_47f5b48ea632d303b95ef7d183a4ab0c
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K19-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G02F1-13
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-94
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-76
filingDate 1988-10-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f7f987300a1fd4c00522fc384e00beab
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_84828525fe42fde48e99b006fc4a881a
publicationDate 1990-04-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H02104562-A
titleOfInvention Optically active biphenyl compound and liquid crystal composition containing the compound
abstract NEW MATERIAL:A compound of the formula (R is 1-18C alkyl, 1-18C alkoxy; A is halogen, OH, 1-18C alkoxy, 1-18C acyloxy; * is asymmetric carbon). n EXAMPLE: (1R,3S)-4'-n-Octyloxybiphenyl-4-carboxylic (3-hydroxy-1,3- dimethylpropyl) ester. n USE: A component for liquid crystal. A component for ferroelectric liquid crystal composition with response speed of reduced temperature dependency. n PREPARATION: For example, (2R,4R)-pentanediol, 4'-n-octyloxybiphenyl-4- carboxylic acid, and triphenyl phosphine are dissolved in diethyl ether. Then, diethyl azodicarboxylate is added to effect the reaction at room temperature to give the objective compound. n COPYRIGHT: (C)1990,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7745424-B2
priorityDate 1988-10-13-04:00^^<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: 23.