http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H08269054-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d5d04736b0b882a4f5a1e0e0e4cd8cbb
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G02F1-13
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K19-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K19-54
filingDate 1995-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ace46f91041ea902659c89f257a58525
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2c066eeb24ebb3215b163fb9ac0eaba7
publicationDate 1996-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H08269054-A
titleOfInvention Optically active compound and liquid crystal composition containing the same
abstract (57) [Summary] (Modified) [Structure] An optically active compound represented by formula (I) and a liquid crystal composition containing the compound. [Wherein, R 1, R 2 is C 1 -C 3 optionally substituted by alkoxy or halogen atom, C 1 -C 18 represents an alkyl group or a C 2 -C 18 alkenyl group (or an alkynyl group) , They may contain an ether bond; the benzene ring has a halogen atom, a C 1 -C 5 (halo) alkyl group, a C 1 -C 5 alkoxy group, -CN,-. It may be substituted with CF 3 ; n is 0 or 1; water represents a chiral carbon atom] [Effect] The compound of the general formula (I) itself has a response rate higher than that of the existing lactone compound. Provides a strong induction liquid crystal material that is extremely fast and has excellent memory properties, and when mixed with a known liquid crystal compound, exhibits strong induction electric properties in a wide temperature range and improves spontaneous polarization, viscosity, responsiveness, etc. The above liquid crystal composition is provided.
priorityDate 1995-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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