http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-106083897-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K2211-1044 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K2211-1088 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N21-643 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D519-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K11-06 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K11-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D519-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N21-64 |
| filingDate | 2016-05-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2019-02-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2019-02-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-106083897-B |
| titleOfInvention | Imidazopyridine rhodamine salicylide Cu-like ion ratio fluorescent probe and its application |
| abstract | The invention discloses a kind of imidazo [1,5-a] pyridine-rhodamine salicylide Cu-like ion ratio fluorescent probe and its application, the probe is the rhodamine salicylide that imidazo [1,5-a] pyridine replaces, and chemical structural formula is as the formula (1).Fluorescence probe of the invention is in ethanol solution to Cu 2+ Have unique fluorescence selectivity, higher sensitivity and it is stronger resist other ion interference abilities, have huge application prospect. |
| priorityDate | 2016-05-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 51.