Ethyl 4-chloro-5,8-difluoroquinoline-3-carboxylate is a chemical compound characterized by its quinoline structure, which is a bicyclic aromatic compound containing a nitrogen atom. This substance features a carboxylate functional group, which contributes to its reactivity and solubility in various solvents. The presence of chlorine and fluorine substituents on the quinoline ring enhances its biological activity and may influence its pharmacological properties. Typically, compounds like this are of interest in medicinal chemistry due to their potential as drug candidates, particularly in the development of antimicrobial or anticancer agents. The ethyl ester group indicates that it can undergo hydrolysis to form the corresponding carboxylic acid, which may further participate in various chemical reactions. Additionally, the compound's molecular structure suggests it may exhibit unique electronic properties due to the electron-withdrawing effects of the halogen atoms, potentially affecting its interaction with biological targets. Overall, ethyl 4-chloro-5,8-difluoroquinoline-3-carboxylate is a compound of significant interest in both synthetic and medicinal chemistry.

ethyl 4-chloro-5,8-difluoroquinoline-3-carboxylate

193827-70-2: Ethyl 4-chloro-5,8-difluoroquinoline-3-carboxylate is a chemical compound characterized by its quinoline structure, which is a bicyclic aromatic compound containing a nitrogen atom. This substance features a carboxylate functional group, which contributes to its reactivity and solubility in various solvents. The presence of chlorine and fluorine substituents on the quinoline ring enhances its biological activity and may influence its pharmacological properties. Typically, compounds like this are of interest in medicinal chemistry due to their potential as drug candidates, particularly in the development of antimicrobial or anticancer agents. The ethyl ester group indicates that it can undergo hydrolysis to form the corresponding carboxylic acid, which may further participate in various chemical reactions. Additionally, the compound's molecular structure suggests it may exhibit unique electronic properties due to the electron-withdrawing effects of the halogen atoms, potentially affecting its interaction with biological targets. Overall, ethyl 4-chloro-5,8-difluoroquinoline-3-carboxylate is a compound of significant interest in both synthetic and medicinal chemistry.

<p>4-Chloro-5,8-difluoroquinoline-3-carboxylic acid ethyl ester</p>

CAS 193827-70-2

ethyl 4-chloro-5,8-difluoroquinoline-3-carboxylate

4-Chloro-5,8-difluoroquinoline-3-carboxylic acid ethyl ester

Ref: 54-PC407058