3-[5-(4-Bromophenyl)isoxazol-3-yl]propanoic acid, with the CAS number 870703-99-4, is a chemical compound characterized by its unique structural features, including an isoxazole ring and a propanoic acid moiety. The presence of the 4-bromophenyl group contributes to its potential biological activity, as halogenated aromatic compounds often exhibit interesting pharmacological properties. This compound is likely to be a solid at room temperature, given its structural complexity and the presence of multiple functional groups. It may exhibit moderate solubility in polar solvents due to the carboxylic acid group, while its aromatic components could enhance lipophilicity. The isoxazole ring suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting various biological pathways. Additionally, the compound's reactivity may be influenced by the bromine substituent, which can participate in electrophilic aromatic substitution reactions. Overall, 3-[5-(4-bromophenyl)isoxazol-3-yl]propanoic acid represents a compound of interest for further research in organic synthesis and drug development.

3-[5-(4-bromophenyl)isoxazol-3-yl]propanoic acid

870703-99-4: 3-[5-(4-Bromophenyl)isoxazol-3-yl]propanoic acid, with the CAS number 870703-99-4, is a chemical compound characterized by its unique structural features, including an isoxazole ring and a propanoic acid moiety. The presence of the 4-bromophenyl group contributes to its potential biological activity, as halogenated aromatic compounds often exhibit interesting pharmacological properties. This compound is likely to be a solid at room temperature, given its structural complexity and the presence of multiple functional groups. It may exhibit moderate solubility in polar solvents due to the carboxylic acid group, while its aromatic components could enhance lipophilicity. The isoxazole ring suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting various biological pathways. Additionally, the compound's reactivity may be influenced by the bromine substituent, which can participate in electrophilic aromatic substitution reactions. Overall, 3-[5-(4-bromophenyl)isoxazol-3-yl]propanoic acid represents a compound of interest for further research in organic synthesis and drug development.

CAS 870703-99-4

3-[5-(4-bromophenyl)isoxazol-3-yl]propanoic acid

5-(4-Bromophenyl)isoxazole-3-propionic acid

Ref: IN-DA003M5B