http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-660408-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_315d611c240458b1308de8455144105a |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B23-04 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B23-04 |
filingDate | 1949-04-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_923bf6b5f705525fa33090d48afdec86 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3d24cdf456027995e392c541efbfb667 |
publicationDate | 1951-11-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | GB-660408-A |
titleOfInvention | Improvements in or relating to cyanine dyes |
abstract | Meso-substituted cyanine dyes are prepared by reacting an alkyl or aralkyl quaternary salt of a benzthiazole containing a thioether grouping in the 2-position with an alkyl or aralkyl quaternary salt of a benzthiazole containing an alkyl-or aralkyl-substituted methyl group in the 2-position, in the presence of a strong base, which is substantially stronger than pyridine and should be at least as strong as triethylamine. Sodium ethoxide may be used. 3 : 31 : 8-Trimethylcyanine iodide is prepared by boiling together in alcohol 2-ethylbenzthiazole methiodide, 2-methylthiobenzthiazole methiodide, and sodium ethoxide or triethylamine. 3 : 31 - Diethyl - 8 - methylthiacyanine iodide is similarly prepared. Specification 424,559 is referred to. |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4232118-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5082765-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6593172-B2 |
priorityDate | 1949-04-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 34.