N-(4-Bromophenyl)-3-Methyl-N-(m-tolyl)aniline, with the CAS number 203710-89-8, is an organic compound characterized by its complex aromatic structure. It features a brominated phenyl group, which enhances its reactivity and potential applications in various chemical reactions. The presence of both a methyl group and a tolyl group contributes to its hydrophobic properties, influencing its solubility in organic solvents. This compound is likely to exhibit moderate to high thermal stability due to the strength of the aromatic bonds. Additionally, the aniline functional group suggests potential for participation in electrophilic substitution reactions, making it useful in synthetic organic chemistry. Its bromine substituent may also impart unique electronic properties, affecting its reactivity and interactions with other chemical species. Overall, this compound's unique structural features position it as a candidate for applications in pharmaceuticals, agrochemicals, or as an intermediate in organic synthesis. However, specific safety and handling guidelines should be followed due to the presence of bromine and the potential for toxicity associated with aniline derivatives.

N-(4-broMophenyl)-3-Methyl-N-(M-tolyl)aniline

203710-89-8: N-(4-Bromophenyl)-3-Methyl-N-(m-tolyl)aniline, with the CAS number 203710-89-8, is an organic compound characterized by its complex aromatic structure. It features a brominated phenyl group, which enhances its reactivity and potential applications in various chemical reactions. The presence of both a methyl group and a tolyl group contributes to its hydrophobic properties, influencing its solubility in organic solvents. This compound is likely to exhibit moderate to high thermal stability due to the strength of the aromatic bonds. Additionally, the aniline functional group suggests potential for participation in electrophilic substitution reactions, making it useful in synthetic organic chemistry. Its bromine substituent may also impart unique electronic properties, affecting its reactivity and interactions with other chemical species. Overall, this compound's unique structural features position it as a candidate for applications in pharmaceuticals, agrochemicals, or as an intermediate in organic synthesis. However, specific safety and handling guidelines should be followed due to the presence of bromine and the potential for toxicity associated with aniline derivatives.

CAS 203710-89-8

N-(4-broMophenyl)-3-Methyl-N-(M-tolyl)aniline

4-bromo-N,N-bis(3-methylphenyl)aniline

Ref: IN-DA00CFMZ

N-(4-Bromophenyl)-3-methyl-N-(m-tolyl)aniline

Ref: 3B-B5638

N-(4-Bromophenyl)-3-methyl-n-(m-tolyl)aniline

Ref: 10-F696111