B50805
1,4-Bis(5-phenyl-2-oxazolyl)benzene
suitable for scintillation, 98%
Synonym(s):
1,4-Bis(5-phenyl-2-oxazolyl)benzene, 2,2′-p-Phenylene-bis(5-phenyloxazole), Di(phenyl-5-oxazolyl-2)-1,4-benzene, POPOP
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About This Item
Empirical Formula (Hill Notation):
C24H16N2O2
CAS Number:
Molecular Weight:
364.40
Beilstein:
325741
MDL number:
UNSPSC Code:
41116105
PubChem Substance ID:
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Assay
98%
mp
242-246 °C (lit.)
suitability
suitable for scintillation
SMILES string
c1ccc(cc1)-c2cnc(o2)-c3ccc(cc3)-c4ncc(o4)-c5ccccc5
InChI
1S/C24H16N2O2/c1-3-7-17(8-4-1)21-15-25-23(27-21)19-11-13-20(14-12-19)24-26-16-22(28-24)18-9-5-2-6-10-18/h1-16H
InChI key
MASVCBBIUQRUKL-UHFFFAOYSA-N
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General description
1,4-Bis(5-phenyl-2-oxazolyl)benzene (POPOP) is a scintillation luminophore. It is commonly used as a secondary wavelength shifter. The photochemical and photophysical studies of POPOP in different solvents have been reported.
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New solution-processable carbazole derivatives as deep blue emitters for organic light-emitting diodes.
Reig M, et al.
Royal Society of Chemistry Advances, 6(11), 9247-9253 (2016)
Investigation of the physical and the optical properties of various base solvents for the liquid scintillator in a neutrino detector.
So SH, et al.
The Journal of the Korean Physical Society, 62(1), 26-33 (2013)
J Hedstrom et al.
Biochemistry, 27(17), 6203-6208 (1988-08-23)
Measurements of homogeneous and heterogeneous fluorescence intensity decays using a hybrid time-correlated single photon counting/multifrequency phase fluorometer are reported. A trio of fluorophores exhibiting a range of decay profiles was selected. p-Terphenyl, 1,4-bis[2-(4-methyl-5-phenyloxazolyl)]benzene [(Me)2POPOP], and p-bis[2-(5-phenyloxazolyl)]benzene (POPOP), commonly used reference
Zheng-Min Yang et al.
Journal of labelled compounds & radiopharmaceuticals, 61(11), 812-819 (2018-06-14)
ZJ0712, a broad-spectrum fungicidal ingredient of strobilurin, exhibits a high protective and curative activity against plant pathogenic fungi. To support the study on its metabolism, residue, environmental behavior, and fate for safety evaluation, two versions of carbon-14 labeled ZJ0712, methyl
B M Kopriwa
Histochemistry, 68(3), 265-279 (1980-01-01)
Several reports have indicated that scintillators enhance the intensity of radioautographic reactions. If this were the case, the use of scintillators would shorten the exposure time of radioautographs and the production of radioautographs would be accelerated. It was, therefore, decided
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