7-Bromo-3-phenyl-quinolin-2-ol is a chemical compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a bromine atom at the 7-position and a phenyl group at the 3-position contributes to its unique reactivity and potential applications in medicinal chemistry. This compound typically exhibits properties such as moderate solubility in organic solvents and may show varying degrees of solubility in water, depending on the pH. The hydroxyl group at the 2-position can participate in hydrogen bonding, influencing its interaction with biological targets. Additionally, the bromine substituent can enhance the compound's lipophilicity and may play a role in its biological activity, potentially making it a candidate for further research in drug development. Its molecular structure suggests potential applications in areas such as anti-cancer research, antimicrobial activity, or as a fluorescent probe, although specific biological activities would require empirical investigation. Safety data and handling precautions should be observed due to the presence of bromine, which can be hazardous.

7-bromo-3-phenyl-quinolin-2-ol

861872-50-6: 7-Bromo-3-phenyl-quinolin-2-ol is a chemical compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a bromine atom at the 7-position and a phenyl group at the 3-position contributes to its unique reactivity and potential applications in medicinal chemistry. This compound typically exhibits properties such as moderate solubility in organic solvents and may show varying degrees of solubility in water, depending on the pH. The hydroxyl group at the 2-position can participate in hydrogen bonding, influencing its interaction with biological targets. Additionally, the bromine substituent can enhance the compound's lipophilicity and may play a role in its biological activity, potentially making it a candidate for further research in drug development. Its molecular structure suggests potential applications in areas such as anti-cancer research, antimicrobial activity, or as a fluorescent probe, although specific biological activities would require empirical investigation. Safety data and handling precautions should be observed due to the presence of bromine, which can be hazardous.

CAS 861872-50-6

7-bromo-3-phenyl-quinolin-2-ol

7-Bromo-2-hydroxy-3-phenylquinoline

Ref: IN-DA004K66

7-Bromo-2-hydroxy-3-phenylquinoline

Ref: 54-OR309276