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Methyl 1H-pyrrolo[2,3-c]pyridine-3-carboxylate

  • CAS No. 108128-12-7

  • Cat. No. CS-0043710
  • Purity≥97%
  • MDL No.MFCD16036494

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

Methyl 1H-pyrrolo[2,3-c]pyridine-3-carboxylate|CS-0043710

Structure of 108128-12-7

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General Information

  • CAS No. 108128-12-7
  • Cat. No. CS-0043710
  • Purity ≥97%
  • MDL No. MFCD16036494
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₈N₂O₂
  • Molecular Weight 176.17
  • Synonym(s) Methyl 6-azaindole-3-carboxylate
  • SMILES O=C(C1=CNC2=C1C=CN=C2)OC

Description

Methyl 1H-pyrrolo[2,3-c]pyridine-3-carboxylate features a fused heterocyclic core with a strategically positioned ester group enabling direct functionalization. This electron-deficient scaffold integrates readily into synthetic sequences requiring nitrogen-rich frameworks. The methyl ester facilitates downstream transformations without prior activation. The compound exhibits robust stability under standard bench conditions and demonstrates compatibility with diverse reaction environments.

Application

Methyl 1H-pyrrolo[2,3-c]pyridine-3-carboxylate serves as a versatile heterocyclic building block for medicinal chemistry and materials science. Its pyrrolopyridine core enables efficient functionalization at the C3 position via palladium-catalyzed cross-coupling reactions. The ester group facilitates further derivatization, while the scaffold exhibits good bench stability and compatibility with standard synthetic protocols.

Safety Information

Download SDS
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   1.3495
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   1

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