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1H-Pyrrolo[3,2-b]pyridine-6-carbaldehyde

  • CAS No. 1020056-33-0

  • Cat. No. CS-0131047
  • Purity≥97%
  • MDL No.MFCD09859114

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

1H-Pyrrolo[3,2-b]pyridine-6-carbaldehyde|CS-0131047

Structure of 1020056-33-0

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General Information

  • CAS No. 1020056-33-0
  • Cat. No. CS-0131047
  • Purity ≥97%
  • MDL No. MFCD09859114
  • Storage 4°C, protect from light, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₆N₂O
  • Molecular Weight 146.15
  • Synonym(s) 4-Azaindole-6-carboxaldehyde
  • SMILES O=CC1=CN=C2C(NC=C2)=C1

Description

1H-Pyrrolo[3,2-b]pyridine-6-carbaldehyde features a fused heterocyclic core with a reactive aldehyde group at the 6-position, enabling direct incorporation into diverse synthetic scaffolds. This electron-deficient platform facilitates efficient coupling reactions and serves as a key building block in medicinal chemistry and materials science applications.

Application

1H-Pyrrolo[3,2-b]pyridine-6-carbaldehyde serves as a versatile heterocyclic building block for medicinal chemistry and materials science. Its aldehyde functionality enables direct incorporation into diverse scaffolds via reductive amination, Grignard additions, or Wittig olefination. The fused pyrrolopyridine core provides enhanced rigidity and π-conjugation, facilitating applications in kinase inhibitor development and organic semiconductors. Bench-stable and readily purified by flash chromatography, it functions efficiently in multistep syntheses requiring high functional group tolerance.

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 : H315-H319-H335
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-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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