http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-3709916-A

Outgoing Links

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S8-922
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B1-514
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B1-514
filingDate 1970-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1973-01-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_69982f3c78807c4753398abbf6a3631b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1db40966f0c1cf69114a96a515b0f7fe
publicationDate 1973-01-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-3709916-A
titleOfInvention Anthraquinone dyestuffs
abstract DYESTUFF OF THE FORMULA 1-OH,4-(3-(F2-CH-),R-PHENYL-NH-),5,8-DI(X)-ANTHRAQUINONE IN WHICH ONE X DENOTES A HYDROXY GROUP, THE OTHER X IS AN AMINO OR NITRO GROUP, AND R STANDS FOR A HYDROGEN ATOM OR A CHLORINE ATOM, AS WELL AS A PROCESS FOR THE PRODUCTION OF THESE DYESTUFFS CHARACTERISED IN THAT, 4,8-DINITRO-1,5-DIHYDROXY-ANTHRAQUINONE AND OR 4,5-DINITRO-1,8DIHYDROXY-ANTHRAQUINONE IS HEATED WITH ANILINES OF THE FORMULA 3-(F2-CH-),R-ANILINE OPTICALLY IN THE PRESENCE OF INERT ORGANIC DILUENTS, AT TEMPERATURES OF ABOUT 100-200* C., AND THE NITRO GROUP CONTAINING RESULTANT DYESTUFFS ARE OPTIONALLY REDUCED IN KNOWN MANNER.
priorityDate 1969-03-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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