3-Phenylquinolin-2-amine is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of the phenyl group at the 3-position and an amino group at the 2-position contributes to its unique chemical properties. This compound typically exhibits a solid state at room temperature and is often characterized by its moderate solubility in organic solvents, while being less soluble in water. It may display various functional properties, including potential biological activity, making it of interest in medicinal chemistry and drug development. The amino group can participate in hydrogen bonding, influencing its reactivity and interaction with other molecules. Additionally, 3-phenylquinolin-2-amine may exhibit fluorescence, which can be useful in analytical applications. Its synthesis often involves multi-step organic reactions, and it can serve as a precursor for further chemical modifications. As with many organic compounds, safety precautions should be taken when handling it, as it may pose health risks if ingested or inhaled.

3-phenylquinolin-2-amine

36926-84-8: 3-Phenylquinolin-2-amine is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of the phenyl group at the 3-position and an amino group at the 2-position contributes to its unique chemical properties. This compound typically exhibits a solid state at room temperature and is often characterized by its moderate solubility in organic solvents, while being less soluble in water. It may display various functional properties, including potential biological activity, making it of interest in medicinal chemistry and drug development. The amino group can participate in hydrogen bonding, influencing its reactivity and interaction with other molecules. Additionally, 3-phenylquinolin-2-amine may exhibit fluorescence, which can be useful in analytical applications. Its synthesis often involves multi-step organic reactions, and it can serve as a precursor for further chemical modifications. As with many organic compounds, safety precautions should be taken when handling it, as it may pose health risks if ingested or inhaled.

CAS 36926-84-8

3-phenylquinolin-2-amine

2-Amino-3-phenylquinoline

Ref: 54-OR3652