http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S54135786-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5128cfc84a0fb189fceb3cd240c44493 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-12 |
| filingDate | 1978-04-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_adf0bbf13c5a01ad893573b2a1754ad1 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_94789a1dc1577e474c066a61858219fe |
| publicationDate | 1979-10-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-S54135786-A |
| titleOfInvention | 3-(4-oxo-3,4-dihydro-1,2,3-benzotriazinyl)esrer compound |
| abstract | NEW MATERIAL:3-(4-Oxo-3,4-dihydro-1,2,3-benzotriazinyl)ester compound of formula I (R is difunctional aliphatic, alicyclic, or araliphatic hydrocarbon residue, difunctional aromatic ring-containing residue). n EXAMPLE: p-(N-Maleimido)benzoic acid 3-(4-oxo-3,4-dihydro-1,2,3-benzotriazinyl) ester. n USE: Reagent for the effective linking of a sulfhydryl-containing substance with an amino-containing substance. It has functional groups different in the reactivity, and useful for the immobilization of enzyme, or as a reagent for the enzyme antibody method, an intermediate of pesticides, etc. n PROCESS: Reaction of the compound II with the compound III in a solvent such as benzene, THF, etc., in the presence of a dehydrating condensation agent such as dicyclohexyl carbodiimide, etc., at -15W+50°C affords the compound I. n COPYRIGHT: (C)1979,JPO&Japio |
| priorityDate | 1978-04-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 24.