6-Bromo-3-chloro-2,4-difluoroaniline is an organic compound characterized by its aromatic amine structure, which includes a benzene ring substituted with various halogen atoms and an amino group. The presence of bromine, chlorine, and fluorine atoms introduces significant electronegativity and steric effects, influencing the compound's reactivity and physical properties. This compound typically exhibits a solid state at room temperature and may have moderate solubility in polar solvents due to the amino group, while its halogen substituents can enhance lipophilicity. The specific arrangement of the halogens on the benzene ring contributes to its potential applications in pharmaceuticals, agrochemicals, or as an intermediate in organic synthesis. Additionally, the compound's reactivity can be affected by the electron-withdrawing nature of the halogens, which may influence nucleophilic substitution reactions. Safety considerations should be taken into account due to the presence of halogens, which can pose environmental and health risks. Overall, 6-bromo-3-chloro-2,4-difluoroaniline is a compound of interest in various chemical research and industrial applications.

6-bromo-3-chloro-2,4-difluoroaniline

201849-12-9: 6-Bromo-3-chloro-2,4-difluoroaniline is an organic compound characterized by its aromatic amine structure, which includes a benzene ring substituted with various halogen atoms and an amino group. The presence of bromine, chlorine, and fluorine atoms introduces significant electronegativity and steric effects, influencing the compound's reactivity and physical properties. This compound typically exhibits a solid state at room temperature and may have moderate solubility in polar solvents due to the amino group, while its halogen substituents can enhance lipophilicity. The specific arrangement of the halogens on the benzene ring contributes to its potential applications in pharmaceuticals, agrochemicals, or as an intermediate in organic synthesis. Additionally, the compound's reactivity can be affected by the electron-withdrawing nature of the halogens, which may influence nucleophilic substitution reactions. Safety considerations should be taken into account due to the presence of halogens, which can pose environmental and health risks. Overall, 6-bromo-3-chloro-2,4-difluoroaniline is a compound of interest in various chemical research and industrial applications.

6-Bromo-3-chloro-2,4-difluoroaniline

<p>6-Bromo-3-chloro-2,4-difluoroaniline</p>

CAS 201849-12-9

6-bromo-3-chloro-2,4-difluoroaniline

6-Bromo-3-chloro-2,4-difluoroaniline

Ref: IN-DA0027VY

6-Bromo-3-chloro-2,4-difluoroaniline

Ref: 54-PC7648