http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H01313455-A
Outgoing Links
Predicate | Object |
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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
Total number of triples: 30.