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CS-W001157 4
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[1,2,4]Triazolo[4,3-a]pyridine-6-carboxylic acid

  • CAS No. 933708-92-0

  • Cat. No. CS-W005345
  • Molecule weightNone
  • Purity≥98%
  • MDL No.MFCD07376943

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

[1,2,4]Triazolo[4,3-a]pyridine-6-carboxylic acid|CS-W005345

Structure of 933708-92-0

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General Information

  • CAS No. 933708-92-0
  • Cat. No. CS-W005345
  • Purity ≥98%
  • MDL No. MFCD07376943
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₅N₃O₂
  • Molecular Weight None
  • Synonym(s) 1,2,4]Triazolo[4,3-a]pyridine-6-carboxylicaci
  • SMILES O=C(C1=CN2C(C=C1)=NN=C2)O

Description

This [1,2,4]Triazolo[4,3-a]pyridine-6-carboxylic acid features a rigid, electron-deficient heterocyclic core paired with a carboxylic acid handle, enabling direct integration into bioconjugation workflows. The fused triazole-pyridine scaffold imparts high metabolic stability and enhanced solubility under physiological conditions, facilitating use in medicinal chemistry campaigns targeting kinase inhibitors and CNS-active compounds.

Application

[1,2,4]Triazolo[4,3-a]pyridine-6-carboxylic acid serves as a versatile heterocyclic building block for medicinal chemistry and materials science. Its fused triazolopyridine core exhibits robust bench stability and facilitates diverse functionalization at the carboxylic acid and pyridine positions. The molecule enables efficient coupling reactions and participates reliably in standard amide bond formation, enabling rapid access to bioactive scaffolds and functionalized intermediates in high-throughput synthesis workflows.

Safety Information

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Computational Chemistry Data

  • TPSA   67.49
  • LogP   0.4275
  • H_Acceptors   4
  • H_Donors   1
  • Rotatable_Bonds   1

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