http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H01313455-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24aca9ded2638ea793d05360dde7a4a0
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P41-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-76
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-14
filingDate 1988-06-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cf1279d98782c00b7ed8767a8017b2f8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6a48cb8be90afcd3b9f41ff9c47b2ea2
publicationDate 1989-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H01313455-A
titleOfInvention Optically active 1-biphenylyethanol ester derivative and production thereof
abstract NEW MATERIAL:The compound of formula I [R is halogen-substituted methyl or (halogen-containing) 2-20C alkyl; R' is 1-15C alkyl; * represents asymmetric carbon]. n EXAMPLE: (+)-4'-(1-Hexadecanoyloxyethyl)-4-biphenylcarboxylic acid ethyl ester. n USE: An intermediate for organic electronic materials (e.g., liquid crystal compounds), agricultural chemicals, pharmaceuticals, etc. n PREPARATION: The objective optically active 1-biphenylylethanol ester derivative of formula I can be produced by reacting an optically active alcohol of formula II with an aliphatic carboxylic acid of formula R-COOH or its derivative. The reaction is usually carried out in the presence or absence of a solvent (e.g., THF or ethyl ether) and generally in the presence of a catalyst (e.g., dimethylaminopyridine). n COPYRIGHT: (C)1989,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2015361027-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9556103-B2
priorityDate 1988-06-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID702
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21885
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226393434
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14744721
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID412224690
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID297
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458397365
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559581
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393636
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID448145875
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419538410
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID235804734
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559261
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21868444
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID3283

Total number of triples: 30.