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CS-W001157 4
Total: USD 88.00

5-(Bromomethyl)-2-methylpyrimidin-4-amine hydrobromide

  • CAS No. 2908-71-6

  • Cat. No. CS-0089026
  • Purity≥97%
  • MDL No.None

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

5-(Bromomethyl)-2-methylpyrimidin-4-amine hydrobromide|CS-0089026

Structure of 2908-71-6

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General Information

  • CAS No. 2908-71-6
  • Cat. No. CS-0089026
  • Purity ≥97%
  • MDL No. None
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₉Br₂N₃
  • Molecular Weight 282.96
  • Synonym(s) 4-Pyrimidinamine, 5-(bromomethyl)-2-methyl-, monohydrobromide
  • SMILES NC1=NC(C)=NC=C1CBr.[H]Br

Description

5-(Bromomethyl)-2-methylpyrimidin-4-amine hydrobromide features a reactive bromomethyl group at the 5-position, enabling efficient coupling in nucleophilic substitution reactions. The pyrimidine core provides a stable, electron-deficient platform for functionalization. This bench-stable salt facilitates direct incorporation into bioconjugation workflows and small molecule synthesis under standard conditions.

Application

5-(Bromomethyl)-2-methylpyrimidin-4-amine hydrobromide serves as a versatile building block for the synthesis of biologically active heterocycles. The bromomethyl group enables efficient nucleophilic substitution, while the pyrimidine core provides a stable scaffold for further functionalization. Its bench-stable nature and compatibility with common coupling reactions facilitate straightforward incorporation into medicinal chemistry campaigns and API development workflows.

Safety Information

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GHS Pictogram :
GHS No : GHS05
Signal Word : Danger
UN#: 3261
Class : 8
Packing Group : Ⅱ
Hazard Statements : H302-H314
Precautionary Statements : P264-P270-P271-P280-P304+P340-P330-P331-P363-P501

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Computational Chemistry Data

  • TPSA   51.8
  • LogP   1.84002
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   1

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