http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1119306-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_dc2f7134efa50484bb359fda73782848
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G03C1-30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D303-16
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D303-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G03C1-30
filingDate 1967-03-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1968-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1119306-A
titleOfInvention Organic substituted sulphonyl diamides and their use in hardening gelatine
abstract Compounds of the formula <FORM:1119306/C3/1> wherein R1 and R2 represent residues bound to the -CO- group by hetero atoms, the residues being capable of reacting with a compound containing one or more reactive H atoms with the formation of one or more homopolar bonds, e.g. R1 and R2 may be X-R1 where X is -OCH2-NH-CH2-, -OCO-, -NHCO-, -NH-SO2- and R1 is a residue capable of reacting with a compound containing one or more reactive hydrogens to form one or more homopolar bonds, e.g. residues of aldehydes, epoxy compounds, ethylene-imine compounds, N-heterocyclic halogen compounds with a reactive halogen in the a -position to the nitrogen, aliphatic halogen compounds, a ,b -ethylenically unsaturated carboxylic acids, a ,b - or b ,g -ethylenically unsaturated sulphonic acids, a -and b -halogeno-carboxylic acids, b -hydroxy sulphonates or -sulphates of aliphatic carboxylic acids, halides or anhydrides of carboxylic acids and halides of sulphonic acids; Compounds of the invention where R1 contains ethylenic unsaturation may be self-polymerized or copolymerized, for example, with acrylonitrile. An example describes the self-polymerization of CH2=CH.CO.NH.CONH. SO2.NH.CO.NH.CO.CH=CH2 and its copolymerization with acrylonitrile; polymerization is effected by heating in dimethylformamide. The products are suitable as thickening agents.ALSO:Novel compounds of formula <FORM:1119306/C2/1> wherein R1 and R2 each represent a residue bound to the -CO- group by a hetero atom, the residue being capable of reacting with a compound containing one or more mobile H atoms with the formation of one or more homopolar bonds, e.g. R1 and R2 may be X-R1 where X is -OCH2-, -NHCH2-, -OCO-, -NHCO-, -NHSO2-, and R1 is a residue capable of reacting with a compound containing one or more mobile H atoms to form one or more homopoler bonds e.g. residues of aldehydes, epoxy compounds, ethylene-imine compounds, N-heterocyclic halogen compounds with a reactive halogen in the a -position to the nitrogen, aliphatic halogen compounds, a ,b -ethylenically unsaturated carboxylic acids, a ,b - or b ,y-ethylenically unsaturated sulphonic acids, a -and b -halogenocarboxylic acids, b -hydroxy sulphonates or -sulphates of aliphatic carboxylic acids, halides or anhydrides of carboxylic acids and halides of sulphonic acids; are produced by reacting sulphonyl di-isocyanate: O = C = N-SO2-N = C = O, in a molecular ratio of 1:2 with a compound containing a mobile hydrogen atom bound to a hetero atom and a residue capable of reacting with a compound containing one or more mobile hydrogen atoms with the formation of one or more homopoler bonds. An alternative method of preparation consists of reacting sulphamide (H2N-SO2-NH2) with acylisocyanates, chlorocarbonic acid esters, or carbamic acid chlorides in a molecular ratio of 1:2 in one or two reaction stages. Another method consists of reacting sulphonyl-bis-carbamic acid esters, with compounds containing amino groups. 2-Carbamoylmethylamino-4,6-dichloro-triazine is prepared from cyanuric chloride and aminoacetamide.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5667960-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4071351-A
priorityDate 1966-04-12-04:00^^<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/CID7855
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414672174
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415764006
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457570881
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458392451
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419531073
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID407992904
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID154333593
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID77898
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6228
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID19785663
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID82267
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7954
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID69020
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458396227
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419527198
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID153846234
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419556970
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID947
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID68048
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419490115
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID432413132
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID431638010
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419550170
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559494
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419523829
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID164602
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9033

Total number of triples: 42.