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CS-W001157 4
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5-Bromo-1H-pyrazolo[3,4-b]pyridine-3-carbaldehyde

  • CAS No. 916326-37-9

  • Cat. No. CS-0040689
  • Purity≥97%
  • MDL No.None

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

5-Bromo-1H-pyrazolo[3,4-b]pyridine-3-carbaldehyde|CS-0040689

Structure of 916326-37-9

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General Information

  • CAS No. 916326-37-9
  • Cat. No. CS-0040689
  • Purity ≥97%
  • MDL No. None
  • Storage -20°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₄BrN₃O
  • Molecular Weight 226.03
  • Synonym(s) 5-bromo-2H-pyrazolo[3,4-b]pyridine-3-carbaldehyde
  • SMILES O=CC1=NNC2=NC=C(Br)C=C21

Description

5-Bromo-1H-pyrazolo[3,4-b]pyridine-3-carbaldehyde features a brominated pyrazolopyridine core paired with an aldehyde handle, enabling direct conjugation in synthetic workflows. The electron-deficient heterocycle supports efficient transition-metal-catalyzed coupling, while the aldehyde group facilitates rapid derivatization under mild conditions. This scaffold integrates readily into bioactive molecule design and advanced materials synthesis.

Application

5-Bromo-1H-pyrazolo[3,4-b]pyridine-3-carbaldehyde serves as a versatile building block for constructing biologically relevant heterocyclic scaffolds. The bromo and aldehyde functionalities enable sequential cross-coupling and functionalization reactions, facilitating access to diverse pyrazolopyridine derivatives. Its bench-stable nature and compatibility with palladium-catalyzed transformations support efficient synthesis in medicinal chemistry 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-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   58.64
  • LogP   1.5329
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   1

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