8-Chloro-6-fluoro-quinoline is a heterocyclic organic compound characterized by a quinoline backbone, which consists of a fused benzene and pyridine ring. The presence of chlorine and fluorine substituents at the 8 and 6 positions, respectively, contributes to its unique chemical properties and potential biological activity. This compound typically exhibits a pale yellow to light brown appearance and is soluble in organic solvents. Its molecular structure allows for various interactions, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The chlorine and fluorine atoms can influence the compound's lipophilicity, reactivity, and overall pharmacokinetic properties. Additionally, 8-chloro-6-fluoro-quinoline may exhibit antimicrobial or antitumor activities, which are common attributes of quinoline derivatives. Safety and handling precautions should be observed, as with many halogenated compounds, due to potential toxicity and environmental concerns. Overall, this compound represents a significant area of study in synthetic organic chemistry and drug development.

8-chloro-6-fluoro-quinoline

22319-88-6: 8-Chloro-6-fluoro-quinoline is a heterocyclic organic compound characterized by a quinoline backbone, which consists of a fused benzene and pyridine ring. The presence of chlorine and fluorine substituents at the 8 and 6 positions, respectively, contributes to its unique chemical properties and potential biological activity. This compound typically exhibits a pale yellow to light brown appearance and is soluble in organic solvents. Its molecular structure allows for various interactions, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The chlorine and fluorine atoms can influence the compound's lipophilicity, reactivity, and overall pharmacokinetic properties. Additionally, 8-chloro-6-fluoro-quinoline may exhibit antimicrobial or antitumor activities, which are common attributes of quinoline derivatives. Safety and handling precautions should be observed, as with many halogenated compounds, due to potential toxicity and environmental concerns. Overall, this compound represents a significant area of study in synthetic organic chemistry and drug development.

CAS 22319-88-6

8-chloro-6-fluoro-quinoline

8-chloro-6-fluoroquinoline

Ref: IN-DA00BIN1

8-Chloro-6-fluoroquinoline

Ref: 10-F630731

8-Chloro-6-fluoroquinoline

Ref: 3D-XAA31988