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CS-W001157 4
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6-Bromo-[1,2,3]triazolo[1,5-a]pyridine

  • CAS No. 192642-82-3

  • Cat. No. CS-0181051
  • Purity≥96%
  • MDL No.MFCD18906775

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

6-Bromo-[1,2,3]triazolo[1,5-a]pyridine|CS-0181051

Structure of 192642-82-3

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General Information

  • CAS No. 192642-82-3
  • Cat. No. CS-0181051
  • Purity ≥96%
  • MDL No. MFCD18906775
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₄BrN₃
  • Molecular Weight 198.02
  • Synonym(s) 6-bromotriazolo[1,5-a]pyridine
  • SMILES BrC1=CN2C(C=C1)=CN=N2

Description

6-Bromo-[1,2,3]triazolo[1,5-a]pyridine is a heterocyclic scaffold featuring a brominated triazolopyridine core, offering a reactive handle for transition-metal-catalyzed coupling reactions. This electron-deficient system integrates readily into complex molecular architectures, enabling efficient access to functionalized nitrogen-rich frameworks in medicinal chemistry and materials science applications.

Application

6-Bromo-[1,2,3]triazolo[1,5-a]pyridine serves as a versatile heterocyclic building block for transition-metal-catalyzed cross-coupling reactions. Its bromine substituent enables reliable Suzuki, Stille, and Negishi couplings, facilitating the construction of biaryl and extended π-conjugated systems. The triazolopyridine core exhibits excellent bench stability, tolerates diverse functional groups, and simplifies purification due to its crystalline nature—making it well-suited for medicinal chemistry and materials synthesis workflows.

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   30.19
  • LogP   1.4918
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   0

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