7-Bromo-6-methoxy-5-azaindole is a heterocyclic compound characterized by the presence of both bromine and methoxy functional groups attached to an azaindole framework. The azaindole structure incorporates a nitrogen atom within the indole ring system, which contributes to its unique chemical properties. This compound typically exhibits moderate solubility in organic solvents, and its reactivity can be influenced by the presence of the bromine atom, which can participate in electrophilic substitution reactions. The methoxy group enhances the electron-donating characteristics of the molecule, potentially affecting its biological activity and interaction with various targets. Compounds of this nature are often studied for their potential applications in pharmaceuticals, particularly in the development of drugs targeting specific biological pathways. Additionally, the presence of halogens and methoxy groups can influence the compound's pharmacokinetics, stability, and overall efficacy in medicinal chemistry. As with many heterocycles, the specific characteristics and reactivity of 7-Bromo-6-methoxy-5-azaindole make it a subject of interest in both synthetic and medicinal chemistry research.

7-Bromo-6-methoxy-5-Azaindole

1190314-42-1: 7-Bromo-6-methoxy-5-azaindole is a heterocyclic compound characterized by the presence of both bromine and methoxy functional groups attached to an azaindole framework. The azaindole structure incorporates a nitrogen atom within the indole ring system, which contributes to its unique chemical properties. This compound typically exhibits moderate solubility in organic solvents, and its reactivity can be influenced by the presence of the bromine atom, which can participate in electrophilic substitution reactions. The methoxy group enhances the electron-donating characteristics of the molecule, potentially affecting its biological activity and interaction with various targets. Compounds of this nature are often studied for their potential applications in pharmaceuticals, particularly in the development of drugs targeting specific biological pathways. Additionally, the presence of halogens and methoxy groups can influence the compound's pharmacokinetics, stability, and overall efficacy in medicinal chemistry. As with many heterocycles, the specific characteristics and reactivity of 7-Bromo-6-methoxy-5-azaindole make it a subject of interest in both synthetic and medicinal chemistry research.

CAS 1190314-42-1

7-Bromo-6-methoxy-5-Azaindole

1H-Pyrrolo[3,2-c]pyridine, 7-bromo-6-methoxy-

Ref: IN-DA000HMI

7-Bromo-6-methoxy-5-azaindole

Ref: 54-OR450015

7-Bromo-6-methoxy-1H-pyrrolo[3,2-c]pyridine

Ref: 10-F092004