
CAS 1456-22-0: 5-Hydroxy-3-phenyl-1,2,4-oxadiazole
Formula:C8H6N2O2
InChI:InChI=1S/C8H6N2O2/c11-8-9-7(10-12-8)6-4-2-1-3-5-6/h1-5H,(H,9,10,11)
InChI key:InChIKey=LMBDRBXGTCUBIH-UHFFFAOYSA-N
SMILES:O=C1NC(=NO1)C2=CC=CC=C2
Synonyms:- 1,2,4-Oxadiazol-5(2H)-one, 3-phenyl-
- 1,2,4-Oxdiazol-5-ol, 3-phenyl-
- 3-Phenyl-1,2,4-oxadiazol-5-ol
- 3-Phenyl-2H-1,2,4-oxadiazol-5-one
- 3-Phenyl-4,5-dihydro-1,2,4-oxadiazol-5-one
- 3-Phenyl-5-hydroxy-1,2,4-oxadiazole
- 3-phenyl-1,2,4-oxadiazol-5(2H)-one
- 5-Hydroxy-3-phenyl-1,2,4-oxadiazole
- Δ<sup>2</sup>-1,2,4-Oxadiazolin-5-one, 3-phenyl-
- Δ2-1,2,4-Oxadiazolin-5-one, 3-phenyl-
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Found 4 products.
1,2,4-Oxadiazol-5(2H)-one, 3-phenyl-
CAS:Formula:C8H6N2O2Purity:95%Color and Shape:SolidMolecular weight:162.14543-Phenyl-[1,2,4]oxadiazol-5-ol
CAS:3-Phenyl-[1,2,4]oxadiazol-5-olPurity:95%Molecular weight:162.15g/mol3-Phenyl-[1,2,4]oxadiazol-5-ol
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:162.14799499511723-Phenyl-1,2,4-oxadiazol-5-ol
CAS:3-Phenyl-1,2,4-oxadiazol-5-ol is a thione that has been shown to be conjugated with DNA and RNA. It is also able to form complexes with metal ions. This compound is spectroscopically active and can be used for the evaluation of biomolecules in vitro. 3-Phenyl-1,2,4-oxadiazol-5-ol can be used as an alternative to ethidium bromide for the detection of nucleic acids in agarose gel electrophoresis. It has been shown to inhibit protein synthesis in bacteria by binding to ribosomes and inhibiting protein synthesis.Formula:C8H6N2O2Purity:Min. 95%Molecular weight:162.15 g/mol