http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105669389-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C41-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C37-055 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C39-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C39-38 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C37-055 |
| filingDate | 2016-03-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2018-04-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2018-04-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-105669389-B |
| titleOfInvention | A kind of BINOL derivatives and its preparation method and application |
| abstract | The present invention relates to a kind of BINOL derivatives, the BINOL derivatives have R the or S configurations of compound representated by below formula： Wherein, R 1 , R 2 It is each independently alkyl or containing fluorophenyl, works as R 1 、R 2 Identical and be methyl, ethyl or 3, during 5 two (trifluoromethyl) phenyl, BINOL derivatives have good chiral Recognition effect.The BINOL derivatives of the application can real-time be analyzed, determine chiral amino alcohol absolute configuration, and this method is few using sample size, analysis is quick and precisely, to sample structure not damaged, configuration is determined without complicated chemical reaction, and have the characteristics that with amino alcohol concentration to be measured to increase and Fluorescence Increasing, recognition effect are good. |
| priorityDate | 2016-03-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 77.