2-(2-Chloro-4-formylphenoxy)propanoic acid is a chemical compound characterized by its unique structure, which includes a chloro-substituted aromatic ring and a propanoic acid moiety. This compound features a phenoxy group, indicating that it has an ether linkage between the aromatic ring and the propanoic acid. The presence of the formyl group (–CHO) on the aromatic ring suggests that it can participate in various chemical reactions, such as nucleophilic additions or condensation reactions. The chloro substituent enhances the compound's reactivity and may influence its biological activity. This compound is likely to be soluble in organic solvents and may exhibit moderate solubility in water due to the presence of the carboxylic acid group. Its potential applications could span across pharmaceuticals, agrochemicals, or as an intermediate in organic synthesis, although specific uses would depend on further research into its properties and biological effects. Safety and handling precautions should be observed, as with any chemical substance, particularly those containing halogens and reactive functional groups.

2-(2-chloro-4-formylphenoxy)propanoic acid

812642-71-0: 2-(2-Chloro-4-formylphenoxy)propanoic acid is a chemical compound characterized by its unique structure, which includes a chloro-substituted aromatic ring and a propanoic acid moiety. This compound features a phenoxy group, indicating that it has an ether linkage between the aromatic ring and the propanoic acid. The presence of the formyl group (–CHO) on the aromatic ring suggests that it can participate in various chemical reactions, such as nucleophilic additions or condensation reactions. The chloro substituent enhances the compound's reactivity and may influence its biological activity. This compound is likely to be soluble in organic solvents and may exhibit moderate solubility in water due to the presence of the carboxylic acid group. Its potential applications could span across pharmaceuticals, agrochemicals, or as an intermediate in organic synthesis, although specific uses would depend on further research into its properties and biological effects. Safety and handling precautions should be observed, as with any chemical substance, particularly those containing halogens and reactive functional groups.

CAS 812642-71-0

2-(2-chloro-4-formylphenoxy)propanoic acid

2-(2-Chloro-4-formylphenoxy)propanoic acid

Ref: 3D-MHB64271