N-(4-bromophenyl)benzamide, with the CAS number 2879-83-6, is an organic compound characterized by its amide functional group and aromatic structure. It features a benzamide core, where a bromophenyl group is substituted at the nitrogen atom of the amide. This compound typically appears as a solid at room temperature and is soluble in organic solvents such as ethanol and dimethyl sulfoxide, but may have limited solubility in water due to its hydrophobic aromatic rings. The presence of the bromine atom introduces both steric and electronic effects, which can influence its reactivity and interactions in chemical reactions. N-(4-bromophenyl)benzamide may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its properties, such as melting point and boiling point, can vary based on purity and specific conditions. As with many organic compounds, proper handling and safety precautions are essential due to potential toxicity or reactivity.

N-(4-bromophenyl)benzamide

N-Benzyl-4-bromoaniline is a chemical compound which has minimal reactivity with amines and imines. It is also able to react with aldehydes, ketones, alcohols, esters, and carboxylic acids. The product of the reaction is an aldimine or a secondary amine. This type of reaction was first discovered in 1894 by Emil Fischer. N-Benzyl-4-bromoaniline can be used as a catalyst for hydroboration reactions because it does not react with functional groups that are sensitive to hydroboration such as carbonyl compounds and nitro compounds. 

The reaction mechanism for this type of reaction is an oxidative addition that forms the intermediate enamine. This enamine reacts with the electrophilic partner to form either an imine or an aldimine. The hydroboration then occurs when the hydrogen on BH3 attacks the iminium ion

CAS 2879-83-6: N-(4-bromophenyl)benzamide

N-Benzyl-4-bromoaniline

Ref: 3D-CAA87983

Benzenemethanamine, N-(4-bromophenyl)-

Ref: IN-DA002WHF

N-Benzyl-4-bromoaniline

Ref: 54-OR310080