2-Bromo-3,4-dimethyl-6-nitrobenzenamine is an organic compound characterized by its aromatic structure, which includes a bromine atom, two methyl groups, and a nitro group attached to a benzene ring. The presence of the amino group (-NH2) indicates that it is an aniline derivative, which often contributes to its reactivity and potential applications in dye synthesis and pharmaceuticals. The bromine substituent can serve as a site for further chemical reactions, such as nucleophilic substitution. The nitro group is known for its electron-withdrawing properties, which can influence the compound's reactivity and stability. The methyl groups provide steric hindrance, potentially affecting the compound's interactions with other molecules. Overall, this compound's unique combination of functional groups makes it a valuable intermediate in organic synthesis, particularly in the development of more complex chemical entities. Its specific properties, such as solubility and melting point, would depend on the molecular interactions and the overall structure, which can be further explored through experimental data.

2-Bromo-3,4-dimethyl-6-nitrobenzenamine

22378-67-2: 2-Bromo-3,4-dimethyl-6-nitrobenzenamine, 4-Amino-3-bromo-5-nitro-o-xylene, 3,4-Xylidine, 2-bromo-6-nitro-, 2-Bromo-3,4-dimethyl-6-nitroaniline, Benzenamine, 2-bromo-3,4-dimethyl-6-nitro-

CAS 22378-67-2: 2-Bromo-3,4-dimethyl-6-nitrobenzenamine

2-bromo-3,4-dimethyl-6-nitroaniline

Ref: 3D-XAA37867

2-bromo-3,4-dimethyl-6-nitroaniline

Ref: IN-DA00I4F3

2-Bromo-3,4-dimethyl-6-nitroaniline

Ref: 10-F038764