http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2003054119-A1

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K2323-00
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K19-58
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K19-586
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K19-58
filingDate 2002-04-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1b6e2c5dcc3af899579065f695b1f451
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1bd1a39ff54f1fb4074797a22a73a272
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a57ced9466bbd99988acddf3cbf646bf
publicationDate 2003-03-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2003054119-A1
titleOfInvention Optically active compound and liquid crystal composition containing the compound
abstract An optically active compound of the following general formula (1) useful as a chiral dbpant, and use thereof, n n n wherein each of X and Y is independently a hydrogen atom or a fluorine atom, R is (C 2 H 5 ) 2 CHCH 2 C*H(CH 3 )—or Ph—C*H(CH 3 )—, A is —Ph(W)—COO—Ph—, —Ph—Ph—COO—, —Cy—COO—Ph—, —Ph(W)—OOC—Ph—COO—, —Ph(W)—OOC—Cy—COO—, —Ph(W)—OOC—Np—COO— or —Np—OOC—, in which Ph— is a phenyl group, —Ph— is a 1,4-phenylene group, —Ph(W)— is —Ph— or monofluoro substituted —Ph—, Cy— is a trans-1,4-cyclohexylene group and —Np— is a 2,6-naphthylene group, and C* is an asymmetric carbon. n The optically active compound of the present invention has a large helical twisting power (HTP) of at least 14 and suitably has the property that its induced helical pitch decreases in length with an increase in temperature, so that it has an excellent value as a chiral dopant for a nematic liquid crystal composition.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2011075073-A1
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priorityDate 2001-04-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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