6-Chloro-2-quinolinamine is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a chlorine atom at the 6-position and an amino group at the 2-position contributes to its unique chemical properties. This compound typically appears as a solid and is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its biological activity. It may exhibit properties such as antimicrobial, antitumor, or anti-inflammatory effects, making it of interest in drug discovery. The compound's reactivity can be influenced by the electron-withdrawing nature of the chlorine substituent, which can affect its interaction with biological targets. Additionally, 6-Chloro-2-quinolinamine may undergo various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, depending on the reaction conditions. Safety and handling precautions should be observed, as with many chemical substances, to mitigate any potential hazards associated with its use.

6-Chloro-2-quinolinamine

18672-02-1: 6-Chloro-2-quinolinamine is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a chlorine atom at the 6-position and an amino group at the 2-position contributes to its unique chemical properties. This compound typically appears as a solid and is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its biological activity. It may exhibit properties such as antimicrobial, antitumor, or anti-inflammatory effects, making it of interest in drug discovery. The compound's reactivity can be influenced by the electron-withdrawing nature of the chlorine substituent, which can affect its interaction with biological targets. Additionally, 6-Chloro-2-quinolinamine may undergo various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, depending on the reaction conditions. Safety and handling precautions should be observed, as with many chemical substances, to mitigate any potential hazards associated with its use.

CAS 18672-02-1

6-Chloro-2-quinolinamine

2-Amino-6-chloroquinoline

Ref: IN-DA007S6K

2-Amino-6-chloroquinoline

Ref: 54-OR471112

6-Chloro-2-quinolinamine

Ref: 10-F720829