Ethyl 4-chloro-7-(trifluoromethoxy)quinoline-3-carboxylate is a chemical compound characterized by its quinoline core, which is a bicyclic structure containing a nitrogen atom. This compound features a carboxylate ester functional group, which contributes to its reactivity and solubility properties. The presence of a chloro substituent at the 4-position and a trifluoromethoxy group at the 7-position enhances its biological activity and lipophilicity, making it of interest in medicinal chemistry. The trifluoromethoxy group is particularly notable for its influence on the compound's electronic properties and potential interactions with biological targets. Ethyl 4-chloro-7-(trifluoromethoxy)quinoline-3-carboxylate may exhibit various pharmacological activities, including antimicrobial or anticancer properties, although specific biological data would depend on empirical studies. Its molecular structure suggests potential applications in drug development, particularly in the design of novel therapeutic agents. As with many synthetic compounds, safety and handling precautions are essential due to the presence of halogenated groups, which can pose environmental and health risks.

ethyl 4-chloro-7-(trifluoromethoxy)quinoline-3-carboxylate

890841-23-3: Ethyl 4-chloro-7-(trifluoromethoxy)quinoline-3-carboxylate is a chemical compound characterized by its quinoline core, which is a bicyclic structure containing a nitrogen atom. This compound features a carboxylate ester functional group, which contributes to its reactivity and solubility properties. The presence of a chloro substituent at the 4-position and a trifluoromethoxy group at the 7-position enhances its biological activity and lipophilicity, making it of interest in medicinal chemistry. The trifluoromethoxy group is particularly notable for its influence on the compound's electronic properties and potential interactions with biological targets. Ethyl 4-chloro-7-(trifluoromethoxy)quinoline-3-carboxylate may exhibit various pharmacological activities, including antimicrobial or anticancer properties, although specific biological data would depend on empirical studies. Its molecular structure suggests potential applications in drug development, particularly in the design of novel therapeutic agents. As with many synthetic compounds, safety and handling precautions are essential due to the presence of halogenated groups, which can pose environmental and health risks.

<p>4-Chloro-7-(trifluoromethoxy)quinoline-3-carboxylic acid ethyl ester</p>

CAS 890841-23-3

ethyl 4-chloro-7-(trifluoromethoxy)quinoline-3-carboxylate

4-Chloro-7-(trifluoromethoxy)quinoline-3-carboxylic acid ethyl ester

Ref: 54-PC404610