Benzenamine, 2-bromo-N-phenyl- is an organic compound characterized by the presence of both an amine and a bromine substituent on a benzene ring. It features a bromine atom attached to the second carbon of the benzene ring, while a phenyl group is connected to the nitrogen atom of the amine functional group. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and temperature. It is known for its aromatic properties and can participate in various chemical reactions, including electrophilic substitution due to the electron-donating nature of the amine group. The presence of the bromine atom can also influence its reactivity, making it a useful intermediate in organic synthesis, particularly in the production of pharmaceuticals, dyes, and agrochemicals. Safety precautions should be taken when handling this compound, as it may pose health risks, including skin and respiratory irritation. Proper storage and disposal methods are essential to mitigate environmental impact.

Benzenamine, 2-bromo-N-phenyl-

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2-Bromodiphenylamine

2-Bromo-N-phenylaniline is a carbonylative synthetic that yields acridone and triarylamines. The abundances of electron ionization reactions for this compound are in the range of 1.5 to 3.0%. Dehalogenation reactions have been observed with arylation and amination reactions, but not with carbolines or diarylamines. 2-Bromo-N-phenylaniline has been shown to act as a ligand for metal ions and catalyze amination reactions involving diarylamines.

CAS 61613-22-7: Benzenamine, 2-bromo-N-phenyl-

2-Bromodiphenylamine

Ref: 3B-B5744

2-Bromo-N-phenylaniline

Ref: 3D-LCA61322

2-Bromodiphenylamine

Ref: IN-DA00EBPR

2-Bromo-N-phenylaniline

Ref: 54-OR79469

2-Bromo-N-phenylaniline

Ref: 10-F603151