http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-5359643-B2

Outgoing Links

Predicate Object
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G73-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G73-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G02F1-1337
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-32
filingDate 2009-07-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2013-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-5359643-B2
titleOfInvention Diamine, liquid crystal aligning agent, liquid crystal aligning film, and liquid crystal display element
abstract The present invention is provided to develop a polyamic acid capable of achieving many characteristics (high voltage holding capacity, little remained DC (direct current), high liquid crystal alignability, high rubbing resistance, etc.) required by a liquid crystal (LC) alignment layer. The invention is achieved through a diamine shown by formula (1). In formula (1), Y represents a single bond or a 1-9 C linear alkylene group, and any -CH2- in the alkylene group may be replaced by -O-, -N(CH3)-, 1,4-phenylene, 1,4-cyclohexylene or piperazine-1,4-diyl; n is 0 or 1; and one hydrogen of a benzene ring that the amino group is bonded to may be replaced by -OH. However, when Y is an alkylene and n is 0, -CH2- that the amino group is bonded to is not replaced by -O- or -N(CH3)-.
priorityDate 2008-08-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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