3-[3-(4-Chlorophenyl)-1,2,4-oxadiazol-5-yl]propanoate, with the CAS number 30149-93-0, is a chemical compound characterized by its unique structure that includes an oxadiazole ring and a propanoate moiety. The presence of the 4-chlorophenyl group contributes to its potential biological activity, as halogenated aromatic compounds often exhibit interesting pharmacological properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents, depending on the specific conditions. Its oxadiazole core is known for its stability and potential applications in medicinal chemistry, particularly in the development of anti-inflammatory and antimicrobial agents. The compound's reactivity can be influenced by the functional groups present, making it a candidate for further chemical modifications. Additionally, its synthesis may involve standard organic reactions such as condensation or esterification. Overall, 3-[3-(4-chlorophenyl)-1,2,4-oxadiazol-5-yl]propanoate represents a class of compounds that are of interest in both synthetic and medicinal chemistry.

3-[3-(4-chlorophenyl)-1,2,4-oxadiazol-5-yl]propanoate

30149-93-0: 3-[3-(4-Chlorophenyl)-1,2,4-oxadiazol-5-yl]propanoate, with the CAS number 30149-93-0, is a chemical compound characterized by its unique structure that includes an oxadiazole ring and a propanoate moiety. The presence of the 4-chlorophenyl group contributes to its potential biological activity, as halogenated aromatic compounds often exhibit interesting pharmacological properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents, depending on the specific conditions. Its oxadiazole core is known for its stability and potential applications in medicinal chemistry, particularly in the development of anti-inflammatory and antimicrobial agents. The compound's reactivity can be influenced by the functional groups present, making it a candidate for further chemical modifications. Additionally, its synthesis may involve standard organic reactions such as condensation or esterification. Overall, 3-[3-(4-chlorophenyl)-1,2,4-oxadiazol-5-yl]propanoate represents a class of compounds that are of interest in both synthetic and medicinal chemistry.

CAS 30149-93-0

3-[3-(4-chlorophenyl)-1,2,4-oxadiazol-5-yl]propanoate

3-[3-(4-CHLOROPHENYL)-1,2,4-OXADIAZOL-5-YL]PROPANOIC ACID

Ref: IN-DA00BNPV

3-(3-(4-Chlorophenyl)-1,2,4-oxadiazol-5-yl)propanoic acid

Ref: 54-OR1069483

3-[3-(4-CHLORO-PHENYL)-[1,2,4]OXADIAZOL-5-YL]-PROPIONIC ACID

Ref: 10-F300963