6-Amino-8-chloro-4-(3-chloro-4-fluoro-anilino)quinoline-3-carbonitrile is a synthetic organic compound characterized by its complex molecular structure, which includes a quinoline core substituted with various functional groups. The presence of an amino group at the 6-position and a chloro group at the 8-position contributes to its potential biological activity. The compound also features a carbonitrile group at the 3-position, which can enhance its reactivity and solubility properties. The additional substitution of a 3-chloro-4-fluoro-aniline moiety at the 4-position introduces further diversity in its chemical behavior and potential interactions. This compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry, particularly in the development of therapeutic agents. Its unique combination of halogen and amino functionalities may influence its binding affinity and selectivity towards biological targets. As with many synthetic compounds, its stability, solubility, and reactivity are influenced by the specific arrangement of its substituents, which can be critical for its application in research and industry.

6-amino-8-chloro-4-(3-chloro-4-fluoro-anilino)quinoline-3-carbonitrile

915364-18-0: 6-Amino-8-chloro-4-(3-chloro-4-fluoro-anilino)quinoline-3-carbonitrile is a synthetic organic compound characterized by its complex molecular structure, which includes a quinoline core substituted with various functional groups. The presence of an amino group at the 6-position and a chloro group at the 8-position contributes to its potential biological activity. The compound also features a carbonitrile group at the 3-position, which can enhance its reactivity and solubility properties. The additional substitution of a 3-chloro-4-fluoro-aniline moiety at the 4-position introduces further diversity in its chemical behavior and potential interactions. This compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry, particularly in the development of therapeutic agents. Its unique combination of halogen and amino functionalities may influence its binding affinity and selectivity towards biological targets. As with many synthetic compounds, its stability, solubility, and reactivity are influenced by the specific arrangement of its substituents, which can be critical for its application in research and industry.

CAS 915364-18-0

6-amino-8-chloro-4-(3-chloro-4-fluoro-anilino)quinoline-3-carbonitrile

3-Quinolinecarbonitrile, 6-aMino-8-chloro-4-[(3-chloro-4-fluorophenyl)aMino]-

Ref: IN-DA00GTZO