8-Chloro-2-phenylquinolin-4(1H)-one is a chemical compound characterized by its quinoline structure, which features a fused bicyclic system containing both a benzene and a pyridine ring. The presence of a chloro substituent at the 8-position and a phenyl group at the 2-position contributes to its unique reactivity and potential biological activity. This compound typically exhibits properties such as moderate solubility in organic solvents and limited solubility in water, which is common for many quinoline derivatives. It may display fluorescence, making it useful in various analytical applications. The compound's structure suggests potential interactions with biological targets, which has led to research into its pharmacological properties, including antimicrobial and anticancer activities. Additionally, the presence of the chloro group can influence its electronic properties and reactivity, making it a subject of interest in synthetic organic chemistry. Overall, 8-chloro-2-phenylquinolin-4(1H)-one is a versatile compound with potential applications in medicinal chemistry and material science.

8-chloro-2-phenylquinolin-4(1H)-one

439147-12-3: 8-Chloro-2-phenylquinolin-4(1H)-one is a chemical compound characterized by its quinoline structure, which features a fused bicyclic system containing both a benzene and a pyridine ring. The presence of a chloro substituent at the 8-position and a phenyl group at the 2-position contributes to its unique reactivity and potential biological activity. This compound typically exhibits properties such as moderate solubility in organic solvents and limited solubility in water, which is common for many quinoline derivatives. It may display fluorescence, making it useful in various analytical applications. The compound's structure suggests potential interactions with biological targets, which has led to research into its pharmacological properties, including antimicrobial and anticancer activities. Additionally, the presence of the chloro group can influence its electronic properties and reactivity, making it a subject of interest in synthetic organic chemistry. Overall, 8-chloro-2-phenylquinolin-4(1H)-one is a versatile compound with potential applications in medicinal chemistry and material science.

CAS 439147-12-3

8-chloro-2-phenylquinolin-4(1H)-one

8-Chloro-4-hydroxy-2-phenylquinoline

Ref: 54-OR309301