| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_9e5ac09d7a83e24a7906faa9be8c3b00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c51f3c17021dd88deab7b36f756a27d1 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K19-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-26 |
| filingDate |
1987-01-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d07a3f1105c99ae233790f9a60e11ca3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4f3fccef8c336fc31b4e56a751ea2662
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_85069c2195f9d27df09a4deb02424917
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c08c40fe60a71e122b36079c16cbf513 |
| publicationDate |
1988-07-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
JP-S63170367-A |
| titleOfInvention |
2-phenyl-5-phenylpyrimidine derivative |
| abstract |
NEW MATERIAL:The 2-phenyyl-5-phenylpyrimidine derivative of formula I (R is alkyl or alkoxy; R* is optically active alkyl or acyl having asymmetric carbon). n EXAMPLE: (S)-2-[4-(2-methoxybutoxy)]phenyl-5-(4-n-octyloxy)phenyl-pyrimidine. n USE: A ferroelectric chiral smectic liquid crystal compound. n PREPARATION: The compound of formula I can be produced e.g. by reacting a compound of formula II with a compound of formula III (X is arylsulfonyl or alkylsulfonyl). n COPYRIGHT: (C)1988,JPO&Japio |
| isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0739884-A2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0739884-A3 |
| priorityDate |
1987-01-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |