CAS 725-12-2
:2,5-Diphenyl-1,3,4-oxadiazole
Description:
2,5-Diphenyl-1,3,4-oxadiazole (CAS 725-12-2) is an organic compound characterized by its heterocyclic structure, which includes an oxadiazole ring featuring two phenyl groups at the 2 and 5 positions. This compound is known for its fluorescent properties, making it useful in various applications, including organic light-emitting diodes (OLEDs) and as a fluorescent probe in biochemical assays. It typically exhibits good thermal stability and solubility in organic solvents, which enhances its utility in synthetic and analytical chemistry. The presence of the oxadiazole moiety contributes to its electronic properties, allowing for potential applications in materials science and photonics. Additionally, 2,5-Diphenyl-1,3,4-oxadiazole can participate in various chemical reactions, including cycloadditions and substitutions, making it a versatile building block in organic synthesis. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper laboratory practices.
Formula:C14H10N2O
InChI:InChI=1S/C14H10N2O/c1-3-7-11(8-4-1)13-15-16-14(17-13)12-9-5-2-6-10-12/h1-10H
InChI key:InChIKey=DCJKUXYSYJBBRD-UHFFFAOYSA-N
SMILES:C=1(OC(=NN1)C2=CC=CC=C2)C3=CC=CC=C3
Synonyms:- 1,3,4-Oxadiazole, 2,5-diphenyl-
- 1,3,4-Oxadiazole, 2-5-diphenyl-
- 2,5-Diphenyloxadiazole
- Brn 0170385
- Nsc 53152
- PPD (scintillator)
- 2,5-Diphenyl-1,3,4-oxadiazole
- PPD
- 4-27-00-07212 (Beilstein Handbook Reference)
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Found 5 products.
2,5-Diphenyl-1,3,4-oxadiazole
CAS:Formula:C14H10N2OPurity:95%Color and Shape:SolidMolecular weight:222.24202,5-Diphenyl-1,3,4-Oxadiazole
CAS:2,5-Diphenyl-1,3,4-OxadiazolePurity:98%Molecular weight:222.25g/mol2,5-Diphenyl-1,3,4-oxadiazole
CAS:<p>2,5-Diphenyl-1,3,4-oxadiazole is an aromatic hydrocarbon that has a linear structure. It has been shown to have potent inhibitory activity against rat liver microsomes and human liver. The mechanism of this inhibition is not yet fully understood. However, it has been suggested that the molecule may be acting as a luminophore, absorbing radiation and emitting it in the form of fluorescence. This hypothesis is supported by the observation of a strong fluorescence when 2,5-diphenyl-1,3,4-oxadiazole is irradiated with light of wavelength between 380 nm and 500 nm. 2,5-Diphenyl-1,3,4-oxadiazole may also be acting as an electron donor or acceptor in a transfer reaction with benzoylhydrazone. This reaction generates radicals which react with oxygen to produce singlet oxygen molecules that can react with other radicals</p>Formula:C14H10N2OPurity:Min. 95%Color and Shape:PowderMolecular weight:222.24 g/mol




