7-Bromo-5-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 5 positions, respectively, introduces unique electronic and steric properties that can influence its reactivity and interactions. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents, depending on the specific conditions. Its molecular structure allows for potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the indole moiety's biological significance. The presence of halogens can enhance the compound's lipophilicity and may affect its binding affinity to biological targets. Additionally, 7-bromo-5-fluoro-1H-indole may participate in various chemical reactions, such as nucleophilic substitutions or coupling reactions, making it a valuable intermediate in synthetic organic chemistry. Safety data should be consulted for handling and storage, as halogenated compounds can pose health and environmental risks.

7-bromo-5-fluoro-1H-indole

408355-23-7: 7-Bromo-5-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 5 positions, respectively, introduces unique electronic and steric properties that can influence its reactivity and interactions. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents, depending on the specific conditions. Its molecular structure allows for potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the indole moiety's biological significance. The presence of halogens can enhance the compound's lipophilicity and may affect its binding affinity to biological targets. Additionally, 7-bromo-5-fluoro-1H-indole may participate in various chemical reactions, such as nucleophilic substitutions or coupling reactions, making it a valuable intermediate in synthetic organic chemistry. Safety data should be consulted for handling and storage, as halogenated compounds can pose health and environmental risks.

CAS 408355-23-7

7-bromo-5-fluoro-1H-indole

7-Bromo-5-Fluoroindole

Ref: IN-DA00BXOW

7-Bromo-5-fluoro-1H-indole

Ref: 54-PC7087

7-Bromo-5-fluoro-1H-indole

Ref: 10-F222823