2-Bromo-3-chlorophenylacetonitrile is an organic compound characterized by the presence of both bromine and chlorine substituents on a phenyl ring, along with a nitrile functional group. Its molecular structure features a phenyl group attached to an acetonitrile moiety, which contributes to its reactivity and potential applications in organic synthesis. The presence of halogens (bromine and chlorine) typically enhances the compound's electrophilic properties, making it useful in various chemical reactions, including nucleophilic substitutions and coupling reactions. This compound is likely to be a solid at room temperature, with moderate solubility in organic solvents due to its polar nitrile group. Its reactivity can be influenced by the electronic effects of the halogen substituents, which can stabilize or destabilize intermediates during chemical transformations. Additionally, 2-bromo-3-chlorophenylacetonitrile may have applications in pharmaceuticals or agrochemicals, where halogenated compounds are often explored for their biological activity. Safety data should be consulted for handling and storage, as halogenated compounds can pose health and environmental risks.

2-bromo-3-chlorophenylacetonitrile

1261815-64-8: 2-Bromo-3-chlorophenylacetonitrile is an organic compound characterized by the presence of both bromine and chlorine substituents on a phenyl ring, along with a nitrile functional group. Its molecular structure features a phenyl group attached to an acetonitrile moiety, which contributes to its reactivity and potential applications in organic synthesis. The presence of halogens (bromine and chlorine) typically enhances the compound's electrophilic properties, making it useful in various chemical reactions, including nucleophilic substitutions and coupling reactions. This compound is likely to be a solid at room temperature, with moderate solubility in organic solvents due to its polar nitrile group. Its reactivity can be influenced by the electronic effects of the halogen substituents, which can stabilize or destabilize intermediates during chemical transformations. Additionally, 2-bromo-3-chlorophenylacetonitrile may have applications in pharmaceuticals or agrochemicals, where halogenated compounds are often explored for their biological activity. Safety data should be consulted for handling and storage, as halogenated compounds can pose health and environmental risks.

CAS 1261815-64-8

2-bromo-3-chlorophenylacetonitrile

2-BROMO-3-CHLOROPHENYLACETONITRILE

Ref: 10-F538869