Ethyl 4-(5-chloro-2-thienyl)-4-oxo-butanoate is an organic compound characterized by its ester functional group, which is derived from the reaction of an alcohol (ethanol) and a carboxylic acid. The presence of a thienyl group, specifically a 5-chloro-2-thienyl moiety, indicates that the compound contains a sulfur-containing heterocyclic ring, contributing to its unique chemical properties and potential reactivity. The 4-oxo group suggests that the compound features a carbonyl functional group, which can participate in various chemical reactions, such as nucleophilic additions or condensation reactions. This compound may exhibit biological activity due to its structural features, making it of interest in medicinal chemistry and drug development. Its molecular structure allows for potential interactions with biological targets, which could lead to pharmacological applications. Additionally, the presence of chlorine may influence its solubility and reactivity, making it a candidate for further study in synthetic organic chemistry and related fields.

ethyl 4-(5-chloro-2-thienyl)-4-oxo-butanoate

473694-31-4: Ethyl 4-(5-chloro-2-thienyl)-4-oxo-butanoate is an organic compound characterized by its ester functional group, which is derived from the reaction of an alcohol (ethanol) and a carboxylic acid. The presence of a thienyl group, specifically a 5-chloro-2-thienyl moiety, indicates that the compound contains a sulfur-containing heterocyclic ring, contributing to its unique chemical properties and potential reactivity. The 4-oxo group suggests that the compound features a carbonyl functional group, which can participate in various chemical reactions, such as nucleophilic additions or condensation reactions. This compound may exhibit biological activity due to its structural features, making it of interest in medicinal chemistry and drug development. Its molecular structure allows for potential interactions with biological targets, which could lead to pharmacological applications. Additionally, the presence of chlorine may influence its solubility and reactivity, making it a candidate for further study in synthetic organic chemistry and related fields.

CAS 473694-31-4

ethyl 4-(5-chloro-2-thienyl)-4-oxo-butanoate

Ethyl 4-(5-Chloro-2-thienyl)-4-oxobutanoate

Ref: 10-F208173