7-Fluoro-6-quinolinamine is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a fluorine atom at the 7-position and an amino group at the 6-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the amino group, which can engage in hydrogen bonding. Its molecular structure suggests potential biological activity, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The fluorine substitution can enhance lipophilicity and metabolic stability, which are desirable traits in drug design. Additionally, 7-Fluoro-6-quinolinamine may participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, due to the reactivity of the amino group and the electron-withdrawing nature of the fluorine atom. Overall, this compound's characteristics make it a valuable subject for research in both synthetic and medicinal chemistry.

7-Fluoro-6-quinolinamine

2102411-80-1: 7-Fluoro-6-quinolinamine is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a fluorine atom at the 7-position and an amino group at the 6-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the amino group, which can engage in hydrogen bonding. Its molecular structure suggests potential biological activity, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The fluorine substitution can enhance lipophilicity and metabolic stability, which are desirable traits in drug design. Additionally, 7-Fluoro-6-quinolinamine may participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, due to the reactivity of the amino group and the electron-withdrawing nature of the fluorine atom. Overall, this compound's characteristics make it a valuable subject for research in both synthetic and medicinal chemistry.

CAS 2102411-80-1

7-Fluoro-6-quinolinamine

6-Quinolinamine, 7-fluoro-

Ref: IN-DA01RH92

7-Fluoroquinolin-6-amine

Ref: 54-PC102498

7-FLUOROQUINOLIN-6-AMINE

Ref: 10-F539877