6-Bromo-2,3-dihydro-4-methoxy-1H-indole is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a 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 is typically a solid at room temperature and may exhibit moderate solubility in organic solvents due to its hydrophobic indole framework. The methoxy group enhances its electron-donating characteristics, potentially influencing its reactivity and interactions with biological systems. As a derivative of indole, it may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. The compound's reactivity can be attributed to the presence of the bromine atom, which can participate in nucleophilic substitution reactions. Overall, 6-Bromo-2,3-dihydro-4-methoxy-1H-indole is notable for its structural features and potential applications in various chemical and biological contexts.

6-Bromo-2,3-dihydro-4-methoxy-1H-indole

1000342-58-4: 6-Bromo-2,3-dihydro-4-methoxy-1H-indole, 1H-Indole, 6-bromo-2,3-dihydro-4-methoxy-

CAS 1000342-58-4: 6-Bromo-2,3-dihydro-4-methoxy-1H-indole

1H-Indole, 6-bromo-2,3-dihydro-4-methoxy-

Ref: IN-DA0000JC