6-Fluoro-5-methoxy-1H-indole is a chemical compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of a fluorine atom at the 6-position and a methoxy group at the 5-position contributes to its unique chemical properties. 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 suggests potential biological activity, making it of interest in pharmaceutical research, particularly in the development of compounds with neuroactive or anti-cancer properties. The fluorine substitution can enhance lipophilicity and metabolic stability, while the methoxy group may influence its interaction with biological targets. As with many indole derivatives, 6-fluoro-5-methoxy-1H-indole may participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, making it a versatile building block in organic synthesis. Safety data and handling precautions should be observed, as with all chemical substances, to mitigate any potential hazards associated with its use.

6-fluoro-5-methoxy-1H-indole

63762-83-4: 6-Fluoro-5-methoxy-1H-indole is a chemical compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of a fluorine atom at the 6-position and a methoxy group at the 5-position contributes to its unique chemical properties. 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 suggests potential biological activity, making it of interest in pharmaceutical research, particularly in the development of compounds with neuroactive or anti-cancer properties. The fluorine substitution can enhance lipophilicity and metabolic stability, while the methoxy group may influence its interaction with biological targets. As with many indole derivatives, 6-fluoro-5-methoxy-1H-indole may participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, making it a versatile building block in organic synthesis. Safety data and handling precautions should be observed, as with all chemical substances, to mitigate any potential hazards associated with its use.

CAS 63762-83-4

6-fluoro-5-methoxy-1H-indole

6-Fluoro-5-methoxy-1H-indole

Ref: IN-DA00EFVE

6-Fluoro-5-methoxy-1H-indole

Ref: 54-PC107819

6-Fluoro-5-methoxy-1H-indole

Ref: 10-F244839