http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4110343-A

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S428-914
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B11-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B41M5-1455
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B11-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B41M5-145
filingDate 1977-02-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1978-08-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_797ea44421c10d4fb7b6baf8e2431229
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f439ea3f220388291df956709607b457
publicationDate 1978-08-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4110343-A
titleOfInvention Bisfluoran chromogenic compounds, preparation thereof, and pressure-sensitive copy systems employing same
abstract A substantially colorless bisfluoran chromogenic material having the structural formula ##STR1## wherein R 1 and R 2 each represent an alkyl group; n X and Y each represent a hydrogen atom, a halogen atom, an hydroxyl group, an alkyl group, a nitro group, an amino group, an acyl group, or a carboalkoxy group; n Z represents an oxy radical, a carbonyl group, an alkylene group, an alkylidene group, a sulfonyl group, or a thio radical; and n n represents an integer from 0 to 1. n The bisfluoran compounds are produced by reacting a 4-dialkylamino-2-hydroxy-2'-carboxybenzophenone with a diphenol wherein the diphenol is unsubstituted in at least one of the positions ortho to an hydroxyl group in each of the phenyl rings. The bisfluorans are used in pressure-sensitive copy systems comprising a support bearing microcapsules containing the bisfluorans, alone, or in combination with other color-forming materials.
priorityDate 1973-02-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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