http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1024486-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c7ad58d3c0b071069a8ee0cb8c8ba2e8
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-80
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B57-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B23-0058
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-80
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B57-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B23-01
filingDate 1963-08-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1966-03-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1024486-A
titleOfInvention Naphthalene dyestuffs
abstract The invention comprises dyes having the general formula <FORM:1024486/C4-C5/1> in which R is a hydrogen atom, or an alkyl, aralkyl, cycloalkyl, or aryl radical, R1, R2 and R3 are lower alkyl radicals, X is an acid radical and the aromatic rings as well as the radicals R, R1, R2, R3 may contain non-ionic substituents. The dyes are obtained by reacting compounds of formula <FORM:1024486/C4-C5/2> with indole derivatives of general formula <FORM:1024486/C4-C5/3> in which the symbols have the meanings as above. The reactants are heated in an inert liquid generally at 20-150 DEG C. in presence of an agent causing loss of water from the reactants. The inert liquids include benzene, toluene chloroform, carbon tetrachloride, ethylene chloride, chlorobenzene, dichlorobenzene, dioxane or nitrobenzene, and water removing agents are phosphorus oxychloride, tri- and penta-chloride, thionyl and sulphuryl chlorides and phosgene or mixtures thereof. Friedel Crafts catalysts, e.g. aluminium, zinc, ferric and stannic chlorides or boron triflouride may also be used in the process. Specified non-ionic radicals include fluorine, chlorine, bromine, nitro, amino and acyl radicals, lower alkyl and alkoxy radicals, nitrile groups and non-ionic derivatives of carboxylic acids. In the case when R is hydrogen the dyestuffs obtained as salts can be converted to the corresponding bases which are subsequently quaternized with a compound R1X in which R1 is alkyl, aralkyl or cycloalkyl radical, and X is as above.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6835725-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7041354-B2
priorityDate 1962-08-29-04:00^^<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/CID6371
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID69021906
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419556587
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7416
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID241
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559562
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458392451
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419546200
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID450652499
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458437694
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5943
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22987606
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419546674
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559516
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6356
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID313
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID425199706
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419484319
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID406948316
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID24648
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID450759839
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559219
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5359268
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419512635
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559213
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419524391
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7239
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419527288
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID24408
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID962
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID931
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14917
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID24813
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457814463
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID260
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7964
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23994
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419558836
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419546206
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419526829
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419491804

Total number of triples: 58.