CAS 125292-94-6

3-Quinolinecarboxylic acid, 7-chloro-4-ethoxy-6-fluoro-, ethyl ester

Description:

3-Quinolinecarboxylic acid, 7-chloro-4-ethoxy-6-fluoro-, ethyl ester, identified by CAS number 125292-94-6, is a chemical compound that belongs to the class of quinoline derivatives. This substance features a quinoline ring structure, which is a bicyclic compound composed of a benzene ring fused to a pyridine ring. The presence of various substituents, including a chloro group, an ethoxy group, and a fluoro group, contributes to its unique chemical properties and potential biological activities. The ethyl ester functional group indicates that it can undergo hydrolysis to yield the corresponding carboxylic acid. Such compounds are often studied for their pharmacological properties, including antimicrobial and anti-inflammatory activities. The specific arrangement of substituents on the quinoline ring can significantly influence the compound's reactivity, solubility, and interaction with biological targets. Overall, this compound represents a significant area of interest in medicinal chemistry and drug development.

Formula: C₁₄H₁₃ClFNO₃

3-Quinolinecarboxylic acid, 7-chloro-4-ethoxy-6-fluoro-, ethyl ester

CAS: 125292-94-6

Formula: C₁₄H₁₃ClFNO₃

Color and Shape: Solid

Molecular weight: 297.7093

Ref: IN-DA000NG3

Ethyl 7-Chloro-4-ethoxy-6-fluoro-3,4-dihydroquinoline-3-carboxylate

Controlled Product

CAS: 125292-94-6

Applications Ethyl 7-Chloro-4-ethoxy-6-fluoro-3,4-dihydroquinoline-3-carboxylate is an intermediate in the synthesis of Norfloxacin (N681000), which is a Pefloxacin derivative as antibacterial. Fluorinated quinolone antibacterial. This compound is a contaminant of emerging concern (CECs).
References Koga, H., et al.: J. Med. Chem., 23, 1358 (1980); Hirai, K., et al.: Antimicrob. Agents Chemother., 19, 188 (1981); Holmes, B., et al.: Drugs, 30, 482 (1985)

Formula: C₁₄H₁₃ClFNO₃

Color and Shape: Neat

Molecular weight: 297.71

Ref: TR-C433260