6-Bromo-2,3-difluorobenzenamine is an organic compound characterized by its aromatic structure, which includes a benzene ring substituted with a bromine atom and two fluorine atoms, as well as an amino group (-NH2). The presence of these substituents influences its chemical properties, such as reactivity and polarity. The bromine atom, being a larger halogen, can introduce steric effects, while the fluorine atoms, known for their electronegativity, can enhance the compound's electron-withdrawing characteristics. This compound is likely to exhibit moderate solubility in polar solvents due to the amino group, which can engage in hydrogen bonding. Additionally, the presence of halogens may impart unique reactivity patterns, making it of interest in various synthetic applications, including pharmaceuticals and agrochemicals. Its CAS number, 887579-74-0, allows for precise identification in chemical databases, facilitating research and development efforts. Overall, 6-Bromo-2,3-difluorobenzenamine is a versatile compound with potential applications in organic synthesis and material science.

6-Bromo-2,3-difluorobenzenamine

887579-74-0: Benzenamine, 6-bromo-2,3-difluoro-, 6-Bromo-2,3-difluorobenzenamine

6-Bromo-2,3-difluoroaniline

6-bromo-2,3-difluoroaniline

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CAS 887579-74-0: 6-Bromo-2,3-difluorobenzenamine

6-Bromo-2,3-difluoroaniline

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6-bromo-2,3-difluoroaniline

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6-Bromo-2,3-difluoroaniline

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6-Bromo-2,3-difluoroaniline

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