2-Chloro-7-fluoro-4-methyl-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 specific positions on the quinoline ring significantly influences its chemical properties and reactivity. Typically, compounds like this exhibit moderate to high lipophilicity due to their aromatic structure, which can enhance their ability to penetrate biological membranes. The chlorine atom can introduce polar characteristics, while the fluorine atom often enhances metabolic stability and can influence the compound's electronic properties. This compound may exhibit biological activity, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. Its specific interactions, such as binding affinity to biological targets, would depend on the functional groups and their spatial arrangement. Additionally, the compound's stability, solubility, and reactivity can be influenced by environmental factors such as pH and temperature. Overall, 2-chloro-7-fluoro-4-methyl-quinoline represents a class of compounds with potential applications in drug discovery and development.

2-chloro-7-fluoro-4-methyl-quinoline

271241-25-9: 2-Chloro-7-fluoro-4-methyl-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 specific positions on the quinoline ring significantly influences its chemical properties and reactivity. Typically, compounds like this exhibit moderate to high lipophilicity due to their aromatic structure, which can enhance their ability to penetrate biological membranes. The chlorine atom can introduce polar characteristics, while the fluorine atom often enhances metabolic stability and can influence the compound's electronic properties. This compound may exhibit biological activity, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. Its specific interactions, such as binding affinity to biological targets, would depend on the functional groups and their spatial arrangement. Additionally, the compound's stability, solubility, and reactivity can be influenced by environmental factors such as pH and temperature. Overall, 2-chloro-7-fluoro-4-methyl-quinoline represents a class of compounds with potential applications in drug discovery and development.

CAS 271241-25-9

2-chloro-7-fluoro-4-methyl-quinoline

2-Chloro-7-fluoro-4-methylquinoline

Ref: IN-DA007LVN

7-Fluoro-2-chloro-4-methylquinoline

Ref: 54-PC404619

2-chloro-7-fluoro-4-methylquinoline

Ref: 10-F313794