3-Acetyl-1-benzyl-4-hydroxy-2(1H)-quinolinone, with the CAS number 161185-40-6, is a synthetic organic compound that belongs to the class of quinolinones, which are known for their diverse biological activities. This compound features a quinoline backbone, characterized by a fused aromatic ring system, which contributes to its stability and reactivity. The presence of an acetyl group and a benzyl substituent enhances its lipophilicity, potentially influencing its interaction with biological targets. The hydroxyl group at the 4-position is significant for its potential antioxidant properties and may also participate in hydrogen bonding, affecting the compound's solubility and reactivity. This compound has garnered interest in medicinal chemistry due to its potential pharmacological applications, including antimicrobial and anticancer activities. Its unique structural features make it a subject of study for developing new therapeutic agents. As with many quinolinone derivatives, the specific characteristics, such as solubility, melting point, and spectral properties, can vary based on the conditions and methods used for synthesis and purification.

3-ACETYL-1-BENZYL-4-HYDROXY-2(1H)-QUINOLINONE

161185-40-6: 3-Acetyl-1-benzyl-4-hydroxy-2(1H)-quinolinone, with the CAS number 161185-40-6, is a synthetic organic compound that belongs to the class of quinolinones, which are known for their diverse biological activities. This compound features a quinoline backbone, characterized by a fused aromatic ring system, which contributes to its stability and reactivity. The presence of an acetyl group and a benzyl substituent enhances its lipophilicity, potentially influencing its interaction with biological targets. The hydroxyl group at the 4-position is significant for its potential antioxidant properties and may also participate in hydrogen bonding, affecting the compound's solubility and reactivity. This compound has garnered interest in medicinal chemistry due to its potential pharmacological applications, including antimicrobial and anticancer activities. Its unique structural features make it a subject of study for developing new therapeutic agents. As with many quinolinone derivatives, the specific characteristics, such as solubility, melting point, and spectral properties, can vary based on the conditions and methods used for synthesis and purification.

<p>3-Acetyl-1-benzyl-4-hydroxy-1,2-dihydroquinolin-2-one</p>

CAS 161185-40-6

3-ACETYL-1-BENZYL-4-HYDROXY-2(1H)-QUINOLINONE

3-Acetyl-1-benzyl-4-hydroxy-1,2-dihydroquinolin-2-one

Ref: 54-OR32149