http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-8704912-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c7ad58d3c0b071069a8ee0cb8c8ba2e8 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N47-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D271-07 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D271-07 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D271-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-36 |
| filingDate | 1985-12-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1987-04-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | ES-8704912-A1 |
| titleOfInvention | PROCEDURE FOR OBTAINING N- (3-CHLORO-1,2,4-OXADIA- ZOL-5-IL) -UREAS |
| abstract | PROCEDURE FOR OBTAINING N- (3-CHLORO-1,2,4-OXADIAZOL-5-IL) -UREAS, OF GENERAL FORMULA (I). IN A FIRST STAGE, 2,5-DICHLORO-1,2,4-OXADIAZOL, OF GENERAL FORMULA (II), IS REACTED WITH AQUEOUS AMMONIA AT TEMPERATURES BETWEEN C20 AND B30 DEGREES. IN A SECOND STAGE, 5-AMINO-3-CHLORO-1,2,4-OXADIAZOLE OF GENERAL FORMULA (III), OBTAINED IN THE FIRST STAGE, IS REACTED WITH AN ISOCYANATE OF GENERAL FORMULA (IV), WHERE R MEANS ALKYL, HALOGENOALKYL, CYCLOALKYL OR CYCLOALKYLALKYL. BOTH REACTIONS ARE CARRIED OUT IN THE PRESENCE OF A THINNER AND A CATALYST. APPLICATION AS FUNGICIDES TO FIGHT PESTS. |
| priorityDate | 1984-12-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
| Predicate | Subject |
|---|---|
| isDiscussedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1176 http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419483880 |
Total number of triples: 15.