3-Amino-N-(4-methylphenyl)benzamide, identified by its CAS number 14315-26-5, is an organic compound characterized by the presence of an amino group and a benzamide structure. This compound features a benzene ring substituted with an amino group at the meta position and an N-(4-methylphenyl) group, indicating that a methyl group is attached to the para position of the phenyl ring. The presence of the amino group contributes to its potential as a building block in pharmaceuticals and agrochemicals, as it can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. The compound is likely to exhibit moderate solubility in polar solvents due to its functional groups, and its molecular structure suggests potential for hydrogen bonding, influencing its physical properties such as melting and boiling points. Additionally, the presence of the methyl group may affect its electronic properties and steric hindrance, which can be significant in biological interactions. Overall, 3-amino-N-(4-methylphenyl)benzamide is a versatile compound with potential applications in medicinal chemistry.

3-amino-N-(4-methylphenyl)benzamide

14315-26-5: 3-Amino-N-(4-methylphenyl)benzamide, identified by its CAS number 14315-26-5, is an organic compound characterized by the presence of an amino group and a benzamide structure. This compound features a benzene ring substituted with an amino group at the meta position and an N-(4-methylphenyl) group, indicating that a methyl group is attached to the para position of the phenyl ring. The presence of the amino group contributes to its potential as a building block in pharmaceuticals and agrochemicals, as it can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. The compound is likely to exhibit moderate solubility in polar solvents due to its functional groups, and its molecular structure suggests potential for hydrogen bonding, influencing its physical properties such as melting and boiling points. Additionally, the presence of the methyl group may affect its electronic properties and steric hindrance, which can be significant in biological interactions. Overall, 3-amino-N-(4-methylphenyl)benzamide is a versatile compound with potential applications in medicinal chemistry.

CAS 14315-26-5

3-amino-N-(4-methylphenyl)benzamide

3-Amino-n-(4-methylphenyl)benzamide

Ref: IN-DA007KDP

3-amino-N-(4-methylphenyl)benzamide

Ref: 10-F313985