3,5-Dibromo-N-(4-chlorophenyl)-2-hydroxybenzamide, with the CAS number 6149-62-8, is an organic compound characterized by its complex structure, which includes a benzamide core substituted with bromine and chlorine atoms. This compound features two bromine atoms located at the 3 and 5 positions of the benzene ring, enhancing its reactivity and potential biological activity. The presence of a hydroxyl group at the 2-position contributes to its solubility in polar solvents and may influence its interaction with biological targets. The 4-chlorophenyl group attached to the nitrogen atom of the amide enhances the compound's lipophilicity, potentially affecting its pharmacokinetic properties. This compound may exhibit various biological activities, making it of interest in medicinal chemistry and drug development. Its unique combination of halogen substituents and functional groups suggests potential applications in fields such as agrochemicals or pharmaceuticals, although specific biological effects would require further investigation. Safety and handling precautions should be observed due to the presence of halogens, which can pose environmental and health risks.

3,5-dibromo-N-(4-chlorophenyl)-2-hydroxybenzamide

6149-62-8: 3,5-Dibromo-N-(4-chlorophenyl)-2-hydroxybenzamide, with the CAS number 6149-62-8, is an organic compound characterized by its complex structure, which includes a benzamide core substituted with bromine and chlorine atoms. This compound features two bromine atoms located at the 3 and 5 positions of the benzene ring, enhancing its reactivity and potential biological activity. The presence of a hydroxyl group at the 2-position contributes to its solubility in polar solvents and may influence its interaction with biological targets. The 4-chlorophenyl group attached to the nitrogen atom of the amide enhances the compound's lipophilicity, potentially affecting its pharmacokinetic properties. This compound may exhibit various biological activities, making it of interest in medicinal chemistry and drug development. Its unique combination of halogen substituents and functional groups suggests potential applications in fields such as agrochemicals or pharmaceuticals, although specific biological effects would require further investigation. Safety and handling precautions should be observed due to the presence of halogens, which can pose environmental and health risks.

CAS 6149-62-8

3,5-dibromo-N-(4-chlorophenyl)-2-hydroxybenzamide

3,5-Dibromo-N-(4-chloro-phenyl)-2-hydroxy-benzamide

Ref: 10-F545592