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

  • CAS No. 1234616-83-1

  • Cat. No. CS-0041391
  • Purity≥96%
  • MDL No.MFCD17214374

*For research and further manufacturing use only, not for direct human use.

Methyl 5-bromo-1H-pyrrolo[2,3-b]pyridine-2-carboxylate|CS-0041391

Structure of 1234616-83-1

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General Information

  • CAS No. 1234616-83-1
  • Cat. No. CS-0041391
  • Purity ≥96%
  • MDL No. MFCD17214374
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₇BrN₂O₂
  • Molecular Weight 255.07
  • Synonym(s) Methyl 5-broMo-7-azaindole-2-carboxylate
  • SMILES O=C(C1=CC2=CC(Br)=CN=C2N1)OC

Description

Methyl 5-bromo-1H-pyrrolo[2,3-b]pyridine-2-carboxylate features a brominated pyrrolopyridine core with a methyl ester at the C2 position, enabling direct functionalization in cross-coupling reactions. The electron-deficient heteroaromatic scaffold enhances reactivity in palladium-catalyzed transformations. This bench-stable compound integrates readily into complex molecular architectures under standard conditions.

Application

Methyl 5-bromo-1H-pyrrolo[2,3-b]pyridine-2-carboxylate serves as a versatile building block for constructing biologically relevant heterocyclic scaffolds. The bromo group enables palladium-catalyzed cross-coupling reactions, while the ester functionality supports further derivatization. This compound exhibits good bench stability and facilitates efficient functionalization in standard synthetic workflows, making it well-suited for medicinal chemistry and process development applications.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   54.98
  • LogP   2.112
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   1

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