N-(4-Bromo-2-methylphenyl)acetamide, with the CAS number 24106-05-6, is an organic compound characterized by its amide functional group. It features a brominated aromatic ring, specifically a 4-bromo-2-methylphenyl moiety, which contributes to its chemical properties and reactivity. The presence of the bromine atom enhances its electrophilic character, making it useful in various chemical reactions, including nucleophilic substitutions. The acetamide group provides solubility in polar solvents and can participate in hydrogen bonding, influencing its physical properties such as melting and boiling points. This compound may exhibit biological activity, making it of interest in pharmaceutical research. Its synthesis typically involves the reaction of 4-bromo-2-methylaniline with acetic anhydride or acetyl chloride. As with many organic compounds, safety precautions should be taken when handling it, as it may pose health risks or environmental hazards. Overall, N-(4-Bromo-2-methylphenyl)acetamide is a versatile compound with applications in organic synthesis and medicinal chemistry.

N-(4-Bromo-2-methylphenyl)acetamide

24106-05-6: 4-Acetamido-3-methyl-1-bromobenzene, Acetamide, N-(4-bromo-2-methylphenyl)-, N-(4-Bromo-2-methylphenyl)acetamide, NSC 8062, o-Acetotoluidide, 4′-bromo-, 4-Bromo-2-methylacetanilide

CAS 24106-05-6: N-(4-Bromo-2-methylphenyl)acetamide

4'-Bromo-2'-methylacetanilide

Ref: 3B-B1556

2-Acetamido-5-bromotoluene

Ref: 10-F035757

4-Bromo-2-methylacetanilide

Ref: 54-OR4288

N-(4-bromo-2-methylphenyl)acetamide

Ref: IN-DA003KX6

4'-Bromo-2'-methylacetanilide

Ref: 3D-ZAA10605