3-Quinolinamine, 7-fluoro- is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of an amino group (-NH2) at the 3-position and a fluorine atom at the 7-position of the quinoline ring 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, while its aromatic nature can influence its interactions with other molecules. The fluorine substituent can enhance the compound's lipophilicity and may affect its biological activity, making it of interest in medicinal chemistry and drug development. Additionally, 3-Quinolinamine, 7-fluoro- 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. Its specific applications and behavior in biological systems would depend on further studies and context within pharmaceutical research.

3-Quinolinamine,7-fluoro-

225366-89-2: 3-Quinolinamine, 7-fluoro- is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of an amino group (-NH2) at the 3-position and a fluorine atom at the 7-position of the quinoline ring 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, while its aromatic nature can influence its interactions with other molecules. The fluorine substituent can enhance the compound's lipophilicity and may affect its biological activity, making it of interest in medicinal chemistry and drug development. Additionally, 3-Quinolinamine, 7-fluoro- 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. Its specific applications and behavior in biological systems would depend on further studies and context within pharmaceutical research.

CAS 225366-89-2

3-Quinolinamine,7-fluoro-

3-Quinolinamine,7-fluoro-(9CI)

Ref: IN-DA00BJ4J

7-Fluoroquinolin-3-amine

Ref: 54-PC102412

7-FLUOROQUINOLIN-3-AMINE

Ref: 10-F305844