6-Chloro-2-pyridin-2-ylquinoline-4-carboxylic acid is a chemical compound characterized by its complex structure, which includes a quinoline core substituted with a chloro group and a pyridine moiety. This compound typically exhibits properties associated with heterocyclic aromatic compounds, such as moderate solubility in organic solvents and potential solubility in polar solvents, depending on the functional groups present. The presence of the carboxylic acid group suggests acidic properties, allowing it to participate in various chemical reactions, including esterification and amidation. Additionally, the chloro substituent can influence the compound's reactivity and biological activity, potentially enhancing its interaction with biological targets. This compound may be of interest in medicinal chemistry and drug development due to its structural features, which could confer specific pharmacological properties. Its unique combination of functional groups may also allow for diverse applications in organic synthesis and material science. As with many heterocyclic compounds, it may exhibit interesting electronic properties, making it a candidate for further research in various fields.

6-chloro-2-pyridin-2-ylquinoline-4-carboxylic acid

667412-62-6: 6-Chloro-2-pyridin-2-ylquinoline-4-carboxylic acid is a chemical compound characterized by its complex structure, which includes a quinoline core substituted with a chloro group and a pyridine moiety. This compound typically exhibits properties associated with heterocyclic aromatic compounds, such as moderate solubility in organic solvents and potential solubility in polar solvents, depending on the functional groups present. The presence of the carboxylic acid group suggests acidic properties, allowing it to participate in various chemical reactions, including esterification and amidation. Additionally, the chloro substituent can influence the compound's reactivity and biological activity, potentially enhancing its interaction with biological targets. This compound may be of interest in medicinal chemistry and drug development due to its structural features, which could confer specific pharmacological properties. Its unique combination of functional groups may also allow for diverse applications in organic synthesis and material science. As with many heterocyclic compounds, it may exhibit interesting electronic properties, making it a candidate for further research in various fields.

CAS 667412-62-6

6-chloro-2-pyridin-2-ylquinoline-4-carboxylic acid

6-chloro-2-pyridin-2-ylquinoline-4-carboxylic acid

Ref: IN-DA00FLNR

6-chloro-2-pyridin-2-ylquinoline-4-carboxylic acid

Ref: 10-F307483