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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K19-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C245-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-26
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-34
filingDate 1996-03-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_84a39bbc22d5b3b1b0362cc30bfbbbc9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f8d3b3ae7a844d249d31731c4bcd3903
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publicationDate 1997-09-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H09241230-A
titleOfInvention Optically active liquid crystal compound containing azo group
abstract (57) [Summary] (Correction) [Solution] General formula (I) ( Ra : F, C1-20 alkyl optionally substituted with C1-12 alkoxyl or C2-16 alkenyl, X: -O-, -COO-, -OCO-, -OC. OO-, single bond, m: 0, 1, n: 0, 1, 1,4-phenylene optionally substituted with ring A: F, pyrimidine-2,5-diyl, pyridine-2,5-diyl , Trans-1,4-cyclohexylene, ring B, ring C, ring D: F 1,4-phenylene optionally substituted with, ring D may be a single bond when n = 0, ring D may be biphenyl-4,4′-diyl when n = 0, R b : methyl, Ethyl, R c : alkyl of C2-12, R when R b = ethyl a compound represented by c = C3-12 alkyl, *: an asymmetric carbon of (R) or (S), and a liquid crystal composition containing the same. [Effect] It is important as a constituent element of a photocontrollable antiferroelectric liquid crystal device in the state of a compound alone or a mixture with another antiferroelectric liquid crystal.
priorityDate 1996-03-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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