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CS-W001157 4
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4,7-Dibromo-1h-[1,2,3]triazolo[4,5-c]pyridine

  • CAS No. 1590410-83-5

  • Cat. No. CS-0197562
  • Purity≥98%
  • MDL No.None

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

4,7-Dibromo-1h-[1,2,3]triazolo[4,5-c]pyridine|CS-0197562

Structure of 1590410-83-5

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General Information

  • CAS No. 1590410-83-5
  • Cat. No. CS-0197562
  • Purity ≥98%
  • MDL No. None
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₅H₂Br₂N₄
  • Molecular Weight 277.90
  • Synonym(s) None
  • SMILES BrC1=NC=C(Br)C=2NN=NC12

Description

4,7-Dibromo-1H-[1,2,3]triazolo[4,5-c]pyridine features a rigid, electron-deficient heteroaromatic core that facilitates efficient coupling in transition-metal-catalyzed reactions. This dibrominated triazolopyridine serves as a strategic building block for constructing complex nitrogen-rich scaffolds in medicinal chemistry and materials science.

Application

4,7-Dibromo-1H-[1,2,3]triazolo[4,5-c]pyridine serves as a versatile building block for constructing triazolopyridine-based scaffolds in medicinal chemistry and materials science. The dibromo substitution pattern enables efficient palladium-catalyzed cross-coupling reactions, facilitating the assembly of complex heterocycles with high functional group tolerance. Its bench-stable crystalline form simplifies handling and purification, making it well-suited for iterative synthesis workflows in API development and advanced material design.

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-P330-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   54.46
  • LogP   1.8779
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   0

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