5-Bromo-4-azaindole-3-carboxylic acid is a heterocyclic compound characterized by the presence of a bromine atom, an azaindole structure, and a carboxylic acid functional group. The compound features a five-membered ring containing nitrogen, which contributes to its unique chemical properties. The bromine substituent typically enhances the compound's reactivity and can influence its biological activity. The carboxylic acid group provides acidic characteristics, allowing for potential interactions in various chemical environments, including hydrogen bonding and coordination with metal ions. This compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry and drug development. Its structural features suggest potential applications in the synthesis of more complex molecules or as a building block in organic synthesis. Additionally, the presence of the azaindole moiety may impart specific electronic properties, influencing its behavior in biological systems or as a ligand in coordination chemistry. Overall, 5-Bromo-4-azaindole-3-carboxylic acid is a versatile compound with potential applications in various fields of chemistry and biochemistry.

5-Bromo-4-azaindole 3-carboxylic acid

1167056-46-3: 5-Bromo-4-azaindole-3-carboxylic acid is a heterocyclic compound characterized by the presence of a bromine atom, an azaindole structure, and a carboxylic acid functional group. The compound features a five-membered ring containing nitrogen, which contributes to its unique chemical properties. The bromine substituent typically enhances the compound's reactivity and can influence its biological activity. The carboxylic acid group provides acidic characteristics, allowing for potential interactions in various chemical environments, including hydrogen bonding and coordination with metal ions. This compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry and drug development. Its structural features suggest potential applications in the synthesis of more complex molecules or as a building block in organic synthesis. Additionally, the presence of the azaindole moiety may impart specific electronic properties, influencing its behavior in biological systems or as a ligand in coordination chemistry. Overall, 5-Bromo-4-azaindole-3-carboxylic acid is a versatile compound with potential applications in various fields of chemistry and biochemistry.

1H-Pyrrolo[3,2-b]pyridine-3-carboxylic acid, 5-bromo-

5-Bromo-1H-pyrrolo[3,2-b]pyridine-3-carboxylic acid

CAS 1167056-46-3

5-Bromo-4-azaindole 3-carboxylic acid

1H-Pyrrolo[3,2-b]pyridine-3-carboxylic acid, 5-bromo-

Ref: IN-DA000D2W

5-Bromo-1H-pyrrolo[3,2-b]pyridine-3-carboxylic acid

Ref: 54-OR1066106

5-Bromo-1H-pyrrolo[3,2-b]pyridine-3-carboxylic acid

Ref: 10-F228440