CAS 31676-55-8
:5-Phenyl-3-pyridinol
Description:
5-Phenyl-3-pyridinol, with the CAS number 31676-55-8, is an organic compound characterized by its pyridine ring structure substituted with a phenyl group and a hydroxyl group. This compound typically exhibits properties associated with both aromatic and heterocyclic compounds, including potential solubility in organic solvents and moderate polarity due to the presence of the hydroxyl group. The hydroxyl group can participate in hydrogen bonding, influencing its reactivity and interactions with other molecules. 5-Phenyl-3-pyridinol may exhibit biological activity, making it of interest in medicinal chemistry and pharmacology. Its structure allows for various functionalization, which can lead to derivatives with altered properties. Additionally, the compound's stability and reactivity can be influenced by the electronic effects of the phenyl group and the nitrogen atom in the pyridine ring. Overall, 5-Phenyl-3-pyridinol is a versatile compound with potential applications in various fields, including pharmaceuticals and organic synthesis.
Formula:C11H9NO
InChI:InChI=1S/C11H9NO/c13-11-6-10(7-12-8-11)9-4-2-1-3-5-9/h1-8,13H
InChI key:InChIKey=NUTMKQSGPRZCAU-UHFFFAOYSA-N
SMILES:OC1=CC(=CN=C1)C2=CC=CC=C2
Synonyms:- 3-Hydroxy-5-phenylpyridine
- 3-Pyridinol, 5-Phenyl-
- 5-Phenyl-3-pyridinol
- 5-Phenylpyridin-3-ol
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Found 4 products.
5-Phenylpyridin-3-ol, 95%
CAS:Formula:C11H19NOPurity:95%Color and Shape:Off white SolidMolecular weight:171.205-Phenylpyridin-3-ol
CAS:<p>5-Phenylpyridin-3-ol is an organic compound with the formula C8H6O. It is a white solid that is stable in air. 5-Phenylpyridin-3-ol reacts with bromoacetate to give formate, the reaction being catalyzed by base. The synthetic method involves the use of ethyl bromoacetate and ammonium formate in aqueous solution at room temperature.</p>Formula:C11H9NOPurity:Min. 95%Molecular weight:171.19 g/mol
