http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H04159265-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_03d0f52bb4069f8a19d70dcfb697c67a
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K19-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K19-42
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-26
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G02F1-13
filingDate 1990-10-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_626d15ca3abee18fc7a24d0ceeabf573
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e54edc9732aee318938449d1f203ca6d
publicationDate 1992-06-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H04159265-A
titleOfInvention Branched phenylpyrimidine compound and liquid crystal composition containing the same
abstract NEW MATERIAL:A compound of formula I (X and Y are each H or methyl, but being not H at the same time; m and n are each 4-20). n EXAMPLE: 5-(8-Methylnonyl)-2-(4-octylphenyl)pyrimidine. n USE: Useful as a component of ferroelectric liquid crystal materials capable of realizing quick response. n PREPARATION: A reaction is made in the presence of sodium alcoholate between an amidine hydrochloride of formula II (R 1 is of formula V) and an alkylmalonic diester into a dihydroxy modification of formula III (R 2 is of formula VI), which is then put to halogen substitution using e.g. phosphorus oxychloride. Thence, the resulting dichlorinated modification of formula IV is dehalogenated in the presence of a base, thus giving the objective compound of the formula I. n COPYRIGHT: (C)1992,JPO&Japio
priorityDate 1990-10-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 21.