6-Bromo-5-chloro-1H-indole-3-carbaldehyde is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This particular compound features a bromine atom at the 6-position and a chlorine atom at the 5-position of the indole ring, contributing to its unique reactivity and potential applications in medicinal chemistry. The presence of the aldehyde functional group at the 3-position enhances its reactivity, making it a valuable intermediate in organic synthesis. This compound may exhibit biological activity, which can be attributed to the indole framework, known for its presence in various natural products and pharmaceuticals. Its molecular structure allows for potential interactions with biological targets, making it of interest in drug discovery. Additionally, the halogen substituents can influence the compound's electronic properties and solubility, affecting its behavior in different chemical environments. Overall, 6-bromo-5-chloro-1H-indole-3-carbaldehyde is a compound of interest in both synthetic and medicinal chemistry.

6‐bromo‐5‐chloro‐1h‐indole‐3‐carbaldehyde

1781423-16-2: 6-Bromo-5-chloro-1H-indole-3-carbaldehyde is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This particular compound features a bromine atom at the 6-position and a chlorine atom at the 5-position of the indole ring, contributing to its unique reactivity and potential applications in medicinal chemistry. The presence of the aldehyde functional group at the 3-position enhances its reactivity, making it a valuable intermediate in organic synthesis. This compound may exhibit biological activity, which can be attributed to the indole framework, known for its presence in various natural products and pharmaceuticals. Its molecular structure allows for potential interactions with biological targets, making it of interest in drug discovery. Additionally, the halogen substituents can influence the compound's electronic properties and solubility, affecting its behavior in different chemical environments. Overall, 6-bromo-5-chloro-1H-indole-3-carbaldehyde is a compound of interest in both synthetic and medicinal chemistry.

CAS 1781423-16-2

6‐bromo‐5‐chloro‐1h‐indole‐3‐carbaldehyde

1H-Indole-3-carboxaldehyde, 6-bromo-5-chloro-

Ref: IN-DA0025S8

6-BROMO-5-CHLORO-1H-INDOLE-3-CARBALDEHYDE

Ref: 10-F504790