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CAS 1255098-82-8

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Ethyl 5-bromo-1H-pyrrolo[3,2-b]pyridine-2-carboxylate

Description:
Ethyl 5-bromo-1H-pyrrolo[3,2-b]pyridine-2-carboxylate is a heterocyclic organic compound characterized by its pyrrolopyridine structure, which incorporates both a pyridine and a pyrrole ring. The presence of a bromine atom at the 5-position of the pyrrolopyridine framework contributes to its reactivity and potential applications in medicinal chemistry. The ethyl ester functional group at the 2-position enhances its solubility in organic solvents and may influence its biological activity. This compound is typically synthesized through multi-step organic reactions, often involving bromination and esterification processes. It may exhibit interesting pharmacological properties, making it a candidate for further research in drug development. Additionally, its unique structural features may allow for various modifications, leading to derivatives with tailored properties. As with many heterocycles, it may participate in diverse chemical reactions, including nucleophilic substitutions and coupling reactions, which are valuable in synthetic organic chemistry. Safety and handling precautions should be observed due to the presence of bromine and the potential for biological activity.
Formula:C10H9BrN2O2
InChI:InChI=1S/C10H9BrN2O2/c1-2-15-10(14)8-5-7-6(12-8)3-4-9(11)13-7/h3-5,12H,2H2,1H3
InChI key:InChIKey=BDJZZKVOBJHYTD-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C1=CC=2C(N1)=CC=C(Br)N2
Synonyms:
  • 1H-Pyrrolo[3,2-b]pyridine-2-carboxylic acid, 5-bromo-, ethyl ester
  • Ethyl 5-Bromo-4-Azaindole-2-Carboxylate
  • Ethyl 5-bromo-1H-pyrrolo[3,2-b]pyridine-2-carboxylate
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