7-Bromo-6-fluoro-1H-indole is a heterocyclic organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of bromine and fluorine substituents at the 7 and 6 positions, respectively, significantly influences its chemical reactivity and physical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. It is often utilized in medicinal chemistry and research due to its potential biological activity, particularly in the development of pharmaceuticals. The halogen substituents can enhance the compound's lipophilicity and may affect its interaction with biological targets. Additionally, 7-Bromo-6-fluoro-1H-indole can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it a valuable intermediate in synthetic organic chemistry. Safety data should be consulted for handling, as halogenated compounds can pose health risks. Overall, its unique structure and substituents make it a compound of interest in both academic and industrial research settings.

7-Bromo-6-fluoro-1H-indole

1000339-62-7: 7-Bromo-6-fluoro-1H-indole is a heterocyclic organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of bromine and fluorine substituents at the 7 and 6 positions, respectively, significantly influences its chemical reactivity and physical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. It is often utilized in medicinal chemistry and research due to its potential biological activity, particularly in the development of pharmaceuticals. The halogen substituents can enhance the compound's lipophilicity and may affect its interaction with biological targets. Additionally, 7-Bromo-6-fluoro-1H-indole can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it a valuable intermediate in synthetic organic chemistry. Safety data should be consulted for handling, as halogenated compounds can pose health risks. Overall, its unique structure and substituents make it a compound of interest in both academic and industrial research settings.

CAS 1000339-62-7

7-Bromo-6-fluoro-1H-indole

7-Bromo-6-fluoro-1H-indole

Ref: IN-DA0000DH

7-Bromo-6-fluoro-1H-indole

Ref: 54-PC7085

7-Bromo-6-fluoro-1H-indole

Ref: TR-B187255