5-Fluoro-8-quinolinamine is a chemical compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a fluorine atom at the 5-position and an amino group at the 8-position contributes to its unique properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents, depending on the specific conditions. It is of interest in medicinal chemistry due to its potential biological activities, including antimicrobial and anticancer properties. The fluorine substitution can enhance lipophilicity and influence the compound's interaction with biological targets. Additionally, 5-fluoro-8-quinolinamine may participate in various chemical reactions, making it a valuable intermediate in the synthesis of more complex molecules. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken. Overall, this compound represents a significant area of study in drug development and organic synthesis.

5-FLUORO-8-QUINOLINAMINE

161038-18-2: 5-Fluoro-8-quinolinamine is a chemical compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a fluorine atom at the 5-position and an amino group at the 8-position contributes to its unique properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents, depending on the specific conditions. It is of interest in medicinal chemistry due to its potential biological activities, including antimicrobial and anticancer properties. The fluorine substitution can enhance lipophilicity and influence the compound's interaction with biological targets. Additionally, 5-fluoro-8-quinolinamine may participate in various chemical reactions, making it a valuable intermediate in the synthesis of more complex molecules. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken. Overall, this compound represents a significant area of study in drug development and organic synthesis.

CAS 161038-18-2

5-FLUORO-8-QUINOLINAMINE

8-quinolinamine, 5-fluoro-

Ref: IN-DA001VLX

5-Fluoroquinolin-8-amine

Ref: 54-PC48935

5-Fluoroquinolin-8-amine

Ref: 10-F679892