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CS-W001157 4
Total: USD 88.00

6-Bromo-1,2,4-triazin-3-amine

  • CAS No. 69249-22-5

  • Cat. No. CS-0028230
  • Purity≥95%
  • MDL No.MFCD16877209

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

6-Bromo-1,2,4-triazin-3-amine|CS-0028230

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General Information

  • CAS No. 69249-22-5
  • Cat. No. CS-0028230
  • Purity ≥95%
  • MDL No. MFCD16877209
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₃H₃BrN₄
  • Molecular Weight 174.99
  • Synonym(s) 3-Amino-6-bromo-1,2,4-triazine; 3-amine-6-bromo-1,2,4-triazin
  • SMILES NC1=NC=C(Br)N=N1

Description

6-Bromo-1,2,4-triazin-3-amine serves as a key heterocyclic scaffold for constructing bioactive molecules. This bench-stable compound features a bromine substituent at the 6-position and a primary amine group at the 3-position, enabling facile coupling reactions. The electron-deficient triazine core supports nucleophilic substitution and transition-metal-catalyzed functionalization, making it valuable in medicinal chemistry and materials synthesis.

Application

6-Bromo-1,2,4-triazin-3-amine serves as a versatile building block in medicinal chemistry and heterocyclic synthesis. The bromine substituent enables palladium-catalyzed cross-coupling reactions, while the triazinamine core provides sites for derivatization via nucleophilic substitution or condensation. Its bench-stable nature and compatibility with diverse reaction conditions facilitate efficient construction of complex nitrogen-containing scaffolds relevant to pharmaceutical development.

Synthesis

  • Route1

    References

    • US2011/212967 A1, ; Page/Page column 10 ;

Safety Information

Download SDS
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   64.69
  • LogP   0.2163
  • H_Acceptors   4
  • H_Donors   1
  • Rotatable_Bonds   0

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