6-Bromo-4-methoxy-1H-indole is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of a bromine atom at the 6-position and a methoxy group at the 4-position contributes to its unique chemical properties. This compound typically exhibits moderate solubility in organic solvents and may have limited solubility in water due to its hydrophobic indole core. The bromine substituent can enhance the compound's reactivity, making it useful in various chemical reactions, including electrophilic substitutions. The methoxy group can influence the electronic properties of the indole ring, potentially affecting its biological activity. Compounds like 6-Bromo-4-methoxy-1H-indole are of interest in medicinal chemistry and materials science, as they may exhibit pharmacological properties or serve as intermediates in the synthesis of more complex molecules. Safety data should be consulted for handling and storage, as halogenated compounds can pose specific health and environmental risks.

6-Bromo-4-methoxy-1H-indole

393553-57-6: 1H-indole, 6-bromo-4-methoxy-, 6-Bromo-4-methoxyindole,  6-Bromo-4-methoxy-1H-indole, 6-Bromo-4-methoxy-1H-indole

6-Bromo-4-methoxy-1H-indole is an indole that can be synthesized by dearomatization. This compound has been shown to react with nucleophiles, such as thiols and amines, under basic conditions. In the presence of a base, 6-bromoindole reacts with alkyl halides to form 6-bromoindoles. 6-Bromo-4-methoxy-1H-indole has been used in the synthesis of natural products including indoles and Indolizine A.

CAS 393553-57-6: 6-Bromo-4-methoxy-1H-indole

6-Bromo-4-methoxy-1H-indole

Ref: IN-DA0075AU

6-Bromo-4-methoxy-1H-indole

Ref: 3D-TQA55357

6-Bromo-4-methoxy-1H-indole

Ref: 54-OR94891

6-Bromo-4-methoxy-1H-indole

Ref: 10-F235725