6-Chloro-4-methoxyindole is a chemical compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of a chlorine atom at the 6-position and a methoxy group at the 4-position contributes to its unique reactivity and properties. This compound is typically a solid at room temperature and is soluble in organic solvents, reflecting its aromatic nature. It may exhibit biological activity, making it of interest in pharmaceutical research, particularly in the development of potential therapeutic agents. The chlorine substituent can influence the compound's electronic properties, potentially enhancing its interaction with biological targets. Additionally, the methoxy group can affect solubility and stability. As with many indole derivatives, 6-chloro-4-methoxyindole may participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, making it a versatile building block in organic synthesis. Safety data should be consulted for handling and storage, as with any chemical substance.

6-Chloro-4-methoxyindole

117970-23-7: 6-Chloro-4-methoxyindole is a chemical compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of a chlorine atom at the 6-position and a methoxy group at the 4-position contributes to its unique reactivity and properties. This compound is typically a solid at room temperature and is soluble in organic solvents, reflecting its aromatic nature. It may exhibit biological activity, making it of interest in pharmaceutical research, particularly in the development of potential therapeutic agents. The chlorine substituent can influence the compound's electronic properties, potentially enhancing its interaction with biological targets. Additionally, the methoxy group can affect solubility and stability. As with many indole derivatives, 6-chloro-4-methoxyindole may participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, making it a versatile building block in organic synthesis. Safety data should be consulted for handling and storage, as with any chemical substance.

CAS 117970-23-7

6-Chloro-4-methoxyindole

6-Chloro-4-methoxy-1H-indole

Ref: IN-DA007QME

6-Chloro-4-methoxy indole

Ref: 54-OR3685T

6-Chloro-4-methoxy-1H-indole

Ref: 10-F233622