http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-936087-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_cae71083b119f18009470b1882e54e4d |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C205-03 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C205-03 |
filingDate | 1960-11-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_60f4e036bda1333a5b1c747b176b4872 |
publicationDate | 1963-09-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | GB-936087-A |
titleOfInvention | Polynitroolefins and their method of preparation |
abstract | Polynitro olefins of the formula:- <FORM:0936087/IV(a)/1> wherein R is an alkyl or nitro radical and R1 is an alkyl radical, are polymerized.ALSO:The invention comprises polynitro-olefins of the formula:-<FORM:0936087/IV(a)/1> wherein R is an alkyl or nitro radical and R1 is an alkyl radical. The compounds are prepared by dehydrating a nitro alcohol of the formula:- <FORM:0936087/IV(a)/2> wherein R is an alkyl or nitro radical and R1 is an alkyl radical. The compounds are prepared by dehydrating a nitro alcohol of the formula:- <FORM:0936087/IV(a)/3> with phosphorus pentoxide, phosphoric acid, concentrated hydrochloric acid or concentrated sulphuric acid. The dinitro olefins of the above formula may be oxidized to the corresponding dinitro carboxylic acids or may be reacted with bromine or 2,4-dinitrobenzene sulphonyl chloride. |
priorityDate | 1960-11-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 27.