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CS-W001157 4
Total: USD 88.00

2-Bromo-6-(4-isopropyl-4H-1,2,4-triazol-3-yl)pyridine

  • CAS No. 2093329-79-2

  • Cat. No. CS-W020649
  • Molecule weight267.13
  • Purity≥98%
  • MDL No.None

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

2-Bromo-6-(4-isopropyl-4H-1,2,4-triazol-3-yl)pyridine|CS-W020649

Structure of 2093329-79-2

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General Information

  • CAS No. 2093329-79-2
  • Cat. No. CS-W020649
  • Purity ≥98%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₁₁BrN₄
  • Molecular Weight 267.13
  • Synonym(s) 2-bromo-6-[4-(propan-2-yl)-4H-1,2,4-triazol-3-yl]pyridine
  • SMILES CC(N1C(C2=CC=CC(Br)=N2)=NN=C1)C

Description

2-Bromo-6-(4-isopropyl-4H-1,2,4-triazol-3-yl)pyridine features a brominated pyridine core paired with a sterically hindered isopropyl-substituted triazole moiety, enabling robust coupling in transition-metal-catalyzed transformations. This bench-stable scaffold integrates readily into diverse heterocyclic architectures, offering enhanced solubility and predictable reactivity in medicinal chemistry applications.

Application

2-Bromo-6-(4-isopropyl-4H-1,2,4-triazol-3-yl)pyridine serves as a versatile building block for constructing nitrogen-rich heterocyclic scaffolds. The bromopyridine moiety enables palladium-catalyzed cross-coupling reactions, while the 4-isopropyl-1,2,4-triazole group offers enhanced stability and orthogonal reactivity. This compound facilitates the synthesis of biologically relevant triazolylpyridines with improved solubility and metabolic resistance, making it well-suited for medicinal chemistry campaigns requiring robust functional group compatibility and bench-stable intermediates.

Safety Information

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GHS Pictogram :
GHS No : GHS05,GHS07,GHS09
Signal Word : Danger
UN#: 3261
Class : 8
Packing Group : Ⅲ
Hazard Statements : H302-H318-H410
Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501

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Computational Chemistry Data

  • TPSA   43.6
  • LogP   2.6835
  • H_Acceptors   4
  • H_Donors   0
  • Rotatable_Bonds   2

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