Ethyl 4-bromo-1H-pyrrolo[2,3-c]pyridine-2-carboxylate is a chemical compound characterized by its unique pyrrolopyridine structure, which consists of a fused pyrrole and pyridine ring system. The presence of a bromine atom at the 4-position of the pyrrole ring introduces significant electrophilic properties, making it a useful intermediate in various chemical reactions, particularly in medicinal chemistry and organic synthesis. The ethyl ester functional group contributes to its solubility in organic solvents and can participate in esterification and hydrolysis reactions. This compound may exhibit biological activity, potentially serving as a scaffold for the development of pharmaceuticals. Its molecular structure allows for various substitution patterns, which can be explored to enhance its pharmacological properties. Additionally, the compound's stability and reactivity can be influenced by the electronic effects of the bromine substituent and the carboxylate group, making it a subject of interest in both synthetic and applied chemistry.

Ethyl 4-broMo-1H-pyrrolo[2,3-c]pyridine-2-carboxylate

1086392-42-8: Ethyl 4-bromo-1H-pyrrolo[2,3-c]pyridine-2-carboxylate is a chemical compound characterized by its unique pyrrolopyridine structure, which consists of a fused pyrrole and pyridine ring system. The presence of a bromine atom at the 4-position of the pyrrole ring introduces significant electrophilic properties, making it a useful intermediate in various chemical reactions, particularly in medicinal chemistry and organic synthesis. The ethyl ester functional group contributes to its solubility in organic solvents and can participate in esterification and hydrolysis reactions. This compound may exhibit biological activity, potentially serving as a scaffold for the development of pharmaceuticals. Its molecular structure allows for various substitution patterns, which can be explored to enhance its pharmacological properties. Additionally, the compound's stability and reactivity can be influenced by the electronic effects of the bromine substituent and the carboxylate group, making it a subject of interest in both synthetic and applied chemistry.

CAS 1086392-42-8

Ethyl 4-broMo-1H-pyrrolo[2,3-c]pyridine-2-carboxylate

Ethyl 4-bromo-1H-pyrrolo[2,3-c]pyridine-2-carboxylate

Ref: IN-DA007UHE