4-(5-Chloro-2-thienyl)benzoic acid is an organic compound characterized by its aromatic structure, which includes a benzoic acid moiety and a thienyl group substituted with a chlorine atom. The presence of the thienyl ring, a five-membered heterocyclic compound containing sulfur, contributes to its unique chemical properties, including potential reactivity and solubility characteristics. The chlorine substituent enhances the compound's electrophilic nature, which may influence its reactivity in various chemical reactions. This compound is typically used in research and development, particularly in the fields of pharmaceuticals and agrochemicals, due to its potential biological activity. Its molecular structure allows for various functionalization possibilities, making it a versatile building block in synthetic chemistry. Additionally, the presence of the carboxylic acid functional group (-COOH) provides acidic properties, which can affect its solubility in different solvents and its behavior in biological systems. Overall, 4-(5-chloro-2-thienyl)benzoic acid is a compound of interest for its chemical reactivity and potential applications in various scientific fields.

4-(5-chloro-2-thienyl)benzoic acid

290326-23-7: 4-(5-Chloro-2-thienyl)benzoic acid is an organic compound characterized by its aromatic structure, which includes a benzoic acid moiety and a thienyl group substituted with a chlorine atom. The presence of the thienyl ring, a five-membered heterocyclic compound containing sulfur, contributes to its unique chemical properties, including potential reactivity and solubility characteristics. The chlorine substituent enhances the compound's electrophilic nature, which may influence its reactivity in various chemical reactions. This compound is typically used in research and development, particularly in the fields of pharmaceuticals and agrochemicals, due to its potential biological activity. Its molecular structure allows for various functionalization possibilities, making it a versatile building block in synthetic chemistry. Additionally, the presence of the carboxylic acid functional group (-COOH) provides acidic properties, which can affect its solubility in different solvents and its behavior in biological systems. Overall, 4-(5-chloro-2-thienyl)benzoic acid is a compound of interest for its chemical reactivity and potential applications in various scientific fields.

CAS 290326-23-7

4-(5-chloro-2-thienyl)benzoic acid

Benzoic acid, 4-(5-chloro-2-thienyl)-, sodium salt (1:1)

Ref: IN-DA002V9X