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1H-pyrrolo[2,3-c]pyridine-7-carbaldehyde

  • CAS No. 1260385-31-6

  • Cat. No. CS-0338203
  • Purity≥98%
  • MDL No.MFCD18380824

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

1H-pyrrolo[2,3-c]pyridine-7-carbaldehyde|CS-0338203

Structure of 1260385-31-6

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General Information

  • CAS No. 1260385-31-6
  • Cat. No. CS-0338203
  • Purity ≥98%
  • MDL No. MFCD18380824
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₆N₂O
  • Molecular Weight 146.15
  • Synonym(s) 6-Azaindole-7-carboxaldehyde
  • SMILES C1=CN=C(C=O)C2=C1C=CN2

Description

1H-pyrrolo[2,3-c]pyridine-7-carbaldehyde features a fused heterocyclic core with a strategically positioned aldehyde group, enabling direct coupling in cross-coupling and conjugate addition reactions. This electron-deficient scaffold integrates readily into bioactive molecule architectures, offering enhanced stability and predictable reactivity under standard conditions.

Application

1H-pyrrolo[2,3-c]pyridine-7-carbaldehyde serves as a versatile heterocyclic building block for medicinal chemistry and catalytic synthesis. Its aldehyde functionality enables efficient imine formation, reductive amination, and coupling reactions with nucleophiles, facilitating the construction of complex nitrogen-containing scaffolds. The fused pyrrolopyridine core exhibits good bench stability and compatibility with diverse functional groups, making it suitable for iterative synthesis and library generation in drug discovery workflows.

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+H312+H332-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   45.75
  • LogP   1.3754
  • H_Acceptors   2
  • H_Donors   1
  • Rotatable_Bonds   1

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