CAS 14121-97-2

Benzamide, 4-hydroxy-N-phenyl-

Description:

Benzamide, 4-hydroxy-N-phenyl- is an organic compound characterized by the presence of a benzamide functional group with a hydroxyl group and a phenyl substituent. Its molecular structure features a benzene ring attached to an amide group, where the nitrogen is further substituted with a phenyl group. This compound typically exhibits properties such as being a white to off-white solid, and it is soluble in organic solvents like ethanol and acetone, but less soluble in water due to its hydrophobic aromatic components. The hydroxyl group contributes to its potential as a hydrogen bond donor, influencing its reactivity and interactions in various chemical environments. Benzamide derivatives are often studied for their biological activities, including potential pharmaceutical applications, due to their ability to interact with biological targets. Additionally, the compound may undergo typical reactions associated with amides, such as hydrolysis or substitution, depending on the reaction conditions. Overall, Benzamide, 4-hydroxy-N-phenyl- is of interest in both synthetic and medicinal chemistry contexts.

Formula: C₁₃H₁₁NO₂

4-Hydroxy-N-phenylbenzamide

CAS: 14121-97-2

4-Hydroxy-N-phenylbenzamide is an organic solvent that is used as a potentiator in hexane. This compound has been shown to have potentiating effects on the solubility and volatility of hexane, which are important for industrial applications. 4-Hydroxy-N-phenylbenzamide also has carcinogenic properties, which may be due to its ability to induce DNA transfer reactions with nitro groups or due to its ability to react with chloride ions in the presence of human colon carcinoma cells. The carcinogenic effects of this compound are not limited to humans; it also induces cancerous transformation in mice. Impurities found in this compound include 5-hydroxytryptamine (serotonin) and carboxyamide (NH2CONH2).

Formula: C₁₃H₁₁NO₂

Purity: Min. 95%

Molecular weight: 213.23 g/mol

Ref: 3D-PAA12197