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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01T1-204
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K11-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01T1-204
filingDate 1990-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7c43b155f7f856d611cac83236d9ceff
publicationDate 1992-01-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-4023859-A1
titleOfInvention STERICALLY HIDDEN 1,3-DIPHENYL-2-PYRAZOLINE DERIVATIVES
abstract New sterically hindered 1-phenyl-3-mesityl-2-pyrazoline derivs. (I) are of the formula (I) where R1 = electron donor substit.; and R2 = Me, OMe or H. The prepn. of (I) is claimed whereby mesityl vinyl ketone (II) is reacted with a phenylhydrazine deriv. of formula (III). USE/ADVANTAGE - (I) are claimed for use as scintillators. They are useful in large chambers or in polymer scintillation fibres. Their fluoroescence emission and absorption wavelengths are further apart than usual, so that overlap occurs only at very high (I) concns. in soln. The fluorescence quantum yield and decay time are in the favourable ranges of known derivs.
priorityDate 1990-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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