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CS-W001157 4
Total: USD 88.00

6-Iodo-[1,2,4]triazolo[1,5-a]pyridine

  • CAS No. 614750-84-4

  • Cat. No. CS-W012730
  • Purity≥95%
  • MDL No.MFCD06797552

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

6-Iodo-[1,2,4]triazolo[1,5-a]pyridine|CS-W012730

Structure of 614750-84-4

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General Information

  • CAS No. 614750-84-4
  • Cat. No. CS-W012730
  • Purity ≥95%
  • MDL No. MFCD06797552
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₄IN₃
  • Molecular Weight 245.02
  • Synonym(s) 6-Iodo[1,2,4]triazolo[1,5-a]pyridine
  • SMILES IC1=CN2C(C=C1)=NC=N2

Description

6-Iodo-[1,2,4]triazolo[1,5-a]pyridine is a bench-stable heterocyclic scaffold featuring a reactive iodine handle at the C6 position. This electron-deficient triazolopyridine core integrates readily into cross-coupling reactions, enabling efficient access to complex nitrogen-rich architectures in medicinal chemistry and materials science.

Application

6-Iodo-[1,2,4]triazolo[1,5-a]pyridine serves as a versatile heterocyclic building block for transition-metal-catalyzed cross-coupling reactions. Its iodide moiety enables efficient Pd- or Ni-mediated coupling with boronic acids, amines, and thiols, facilitating rapid access to diverse triazolopyridine derivatives. The scaffold exhibits excellent bench stability, mild handling requirements, and compatibility with common functional groups, making it ideal for medicinal chemistry libraries and API intermediate synthesis.

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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   30.19
  • LogP   1.3339
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   0

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