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B50805

Sigma-Aldrich

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:
1806-34-4
Molecular Weight:
364.40
Beilstein:
325741
MDL number:
MFCD00005309
UNSPSC Code:
41116105
PubChem Substance ID:
329773249

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)
Photophysical Parameters, Excitation Energy Transfer, and Photoreactivity of 1,4-Bis (5-phenyl-2-oxazolyl) benzene (POPOP) Laser Dye.
El-Daly SA, et al.
International Journal of Photoenergy, 2012 (2012)
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
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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