852-38-0
Chemical Structure
2-(4-Biphenylyl)-5-phenyl-1,3,4-oxadiazole
- CAS No.: 852-38-0
- Formula:C20H14N2O
- Molecular Weight:298.34
IUPAC Name: 2-([1,1'-biphenyl]-4-yl)-5-phenyl-1,3,4-oxadiazole
InChIKey: WMAXWOOEPJQXEB-UHFFFAOYSA-N
SMILES: C1(C2=CC=C(C3=CC=CC=C3)C=C2)=NN=C(C4=CC=CC=C4)O1
Biological Activity: 2-(4-Biphenylyl)-5-phenyl-1,3,4-oxadiazole is an oxadiazole derivative. 2-(4-Biphenylyl)-5-phenyl-1,3,4-oxadiazole can serve as a fluorescent dye and organic scintillator, functioning as a primary fluor and wavelength shifter in radiation detection systems, nuclear safety, sensors, nonlinear optical converters, and optoelectronic devices. 2-(4-Biphenylyl)-5-phenyl-1,3,4-oxadiazole is used in liquid solutions, liquid and plastic media, aqueous solutions, and solid-state matrices, with applications in UV laser dyes, fluorescence, and scintillation fields[1][2].
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2-(4-Biphenylyl)-5-phenyl-1,3,4-oxadiazole | 2-(4-Biphenylyl)-5-phenyl-1,3,4-oxadiazole is an oxadiazole derivative. 2-(4-Biphenylyl)-5-phenyl-1,3,4-oxadiazole can serve as a fluorescent dye and organic scintillator, functioning as a primary fluor and wavelength shifter in radiation detection systems, nuclear safety, sensors, nonlinear optical converters, and optoelectronic devices. 2-(4-Biphenylyl)-5-phenyl-1,3,4-oxadiazole is used in liquid solutions, liquid and plastic media, aqueous solutions, and solid-state matrices, with applications in UV laser dyes, fluorescence, and scintillation fields. | |||||||||||||||||||||
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References
- [1]. Kaneva N, et al. Synthesis, Characterization, and Photocatalytic Performance of Rare-Earth-Modified ZnO Nanoflowers for Degradation of 2,5-Diphenyl-1,3-oxazole and 2-(4-Biphenyl)-5-phenyl-1,3,4-oxadiazole. Catalysts. 2026;16(7):661.
- [2]. Imanifard F, et al. Synthesis of a Novel 2-Methyl-8-Quinolinol Complex of Zn (II) and Its Use in Organic Light Emitting Diodes (OLEDs) Fabrication. Iran J Chem Chem Eng. 2025;44(1):[Article].
