http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4074999-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_19270b178cd9a8e5903ddba33b689376 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D513-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-90 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D513-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-90 |
| filingDate | 1973-05-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 1978-02-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e01c4f48f08ca4da38fb7f30e5c240bd |
| publicationDate | 1978-02-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | US-4074999-A |
| titleOfInvention | Use of cyclic thiazines as microbiocides |
| abstract | Cyclic thiazines of the formula ##STR1## where the R's are hydrogen or a substituted group such as a hydrocarbon group, i.e., alkyl, etc. and N is a cyclic moiety, Z is S, ##STR2## and X is an anion, are prepared by reacting a cyclic secondary amine salt with a divinyl sulfur compound. These are illustrated by the reaction of piperidine hydrochloride with divinyl sulfone to yield ##STR3## These products have a wide variety of uses including their use as microbiocides, etc. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4720492-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4407670-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4494977-A |
| priorityDate | 1971-02-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 74.