http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CS-264198-B1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_712ac13e55e9440fc8e166f92b697de7 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_9416a7dd1bcef071457ca40fbba0151e |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-71 |
| filingDate | 1987-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6a5074e76c9dd8ecfa6525822817e446 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e1c95480f4541cab924f456f6382d024 |
| publicationDate | 1989-06-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CS-264198-B1 |
| titleOfInvention | 3- (5-nitro-2-furyl) propenylisothiocyanate and its preparation |
| abstract | 3- (5-nitro-2-furyl) propenylisothiocyanate anway of its preparation. The nature of the method of preparationn3- (5-methyl-2-furyl) propenylisothiocyanatenis that 3- (5-nitro-2-furyl) -npropenylbromide is converted by urotropinnto 3- (5-nitro-2-furyl) propenylamine-nthe hydrochloride from which the thiophosgene actsnproduct in the presence of a base.nAnother method of preparation is to actnsilver or lead acid rodanidento 3- (5-nitro-2-furyl) propenyl bromide an3- (5-nitro-2 furylpropenylisothiocyanate isnChromatographically separate from the by-productn3- (5-nitro-2-furyl) propenyl thiocyanate.nThe compound exhibits biological activitynbacteria and has antiprotozoal efficacy.nIt also finds use in preparing new 3-n- (5-nitro-2-furyl) propenyl derivatives.n3- (5-nitro-2-furyl) propenylisothiocyanate isncharacterized by formula 1. |
| priorityDate | 1987-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 54.