http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-101087593-B1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2f953e662f0f4a6aedb6f11302833d60 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C209-62 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C06B33-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C211-24 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C209-32 |
| filingDate | 2010-07-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2011-11-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_299d1a8df1a4761f0f8b6cd53d0ba531 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ff3bf389446928c8dc6fac68f49be391 |
| publicationDate | 2011-11-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | KR-101087593-B1 |
| titleOfInvention | Method for preparing 1,1-diamino-2,2-dinitroethylene |
| abstract | The present invention relates to nitrating 4,6-dihydroxy-2-methylpyrimidine (DHMP) 4,6-dihydroxy-5,5-dinitro-2- (dinitromethylene) -2,5- When 1,1-diamino-2,2-dinitroethylene was prepared by hydrolysis of dihydropyrimidine (DHDNDP), the rapid reaction solution was not generated by adjusting the hydrolysis reaction conditions to elevated temperature conditions. In particular, the present invention relates to a method for preparing 1,1-diamino-2,2-dinitroethylene (DADNE), which can reduce the reaction time without causing eruptions even when the reaction proceeds on a large scale as well as on a small scale. . |
| priorityDate | 2010-07-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 33.