3-Amino-N-(2-phenylethyl)benzamide, identified by its CAS number 81882-72-6, is an organic compound characterized by the presence of an amine group and an amide functional group. This compound features a benzene ring substituted with an amino group at the meta position and an N-(2-phenylethyl) side chain, which contributes to its structural complexity and potential biological activity. The presence of both the amino and amide functionalities suggests that it may engage in hydrogen bonding, influencing its solubility and reactivity. Typically, compounds of this nature may exhibit properties such as moderate to high polarity, depending on the solvent environment, and could potentially interact with biological systems, making them of interest in medicinal chemistry. The compound's molecular structure may also suggest potential applications in pharmaceuticals, particularly in the development of drugs targeting specific receptors or enzymes. However, detailed studies would be necessary to fully elucidate its properties, including its stability, reactivity, and biological effects.

3-amino-N-(2-phenylethyl)benzamide

81882-72-6: 3-Amino-N-(2-phenylethyl)benzamide, identified by its CAS number 81882-72-6, is an organic compound characterized by the presence of an amine group and an amide functional group. This compound features a benzene ring substituted with an amino group at the meta position and an N-(2-phenylethyl) side chain, which contributes to its structural complexity and potential biological activity. The presence of both the amino and amide functionalities suggests that it may engage in hydrogen bonding, influencing its solubility and reactivity. Typically, compounds of this nature may exhibit properties such as moderate to high polarity, depending on the solvent environment, and could potentially interact with biological systems, making them of interest in medicinal chemistry. The compound's molecular structure may also suggest potential applications in pharmaceuticals, particularly in the development of drugs targeting specific receptors or enzymes. However, detailed studies would be necessary to fully elucidate its properties, including its stability, reactivity, and biological effects.

CAS 81882-72-6

3-amino-N-(2-phenylethyl)benzamide