4-Bromo-2,6-difluoro-N,N-dimethyl-benzenemethanamine is an organic compound characterized by its aromatic structure, which includes a benzene ring substituted with a bromine atom and two fluorine atoms at the 2 and 6 positions. The presence of the N,N-dimethyl group indicates that the amine functional group is attached to the benzene ring, contributing to its basicity and potential reactivity. This compound is likely to exhibit properties typical of halogenated amines, such as increased lipophilicity due to the halogen substituents, which can influence its solubility and interaction with biological systems. The bromine and fluorine atoms can also affect the compound's electronic properties, potentially enhancing its reactivity in nucleophilic substitution reactions. Additionally, the presence of multiple electronegative atoms may lead to interesting hydrogen bonding capabilities. Overall, this compound's unique substitution pattern suggests potential applications in pharmaceuticals or materials science, although specific applications would depend on further research into its biological activity and chemical behavior.

4-Bromo-2,6-diflluoro-N,N-dimethyl-benzenemethanamine

1247006-25-2: 4-Bromo-2,6-difluoro-N,N-dimethyl-benzenemethanamine is an organic compound characterized by its aromatic structure, which includes a benzene ring substituted with a bromine atom and two fluorine atoms at the 2 and 6 positions. The presence of the N,N-dimethyl group indicates that the amine functional group is attached to the benzene ring, contributing to its basicity and potential reactivity. This compound is likely to exhibit properties typical of halogenated amines, such as increased lipophilicity due to the halogen substituents, which can influence its solubility and interaction with biological systems. The bromine and fluorine atoms can also affect the compound's electronic properties, potentially enhancing its reactivity in nucleophilic substitution reactions. Additionally, the presence of multiple electronegative atoms may lead to interesting hydrogen bonding capabilities. Overall, this compound's unique substitution pattern suggests potential applications in pharmaceuticals or materials science, although specific applications would depend on further research into its biological activity and chemical behavior.

CAS 1247006-25-2

4-Bromo-2,6-diflluoro-N,N-dimethyl-benzenemethanamine

1-(4-Bromo-2,6-difluorophenyl)-N,N-dimethylmethanamine

Ref: IN-DA01DNMQ