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CS-W001157 4
Total: USD 88.00

2-(Bromomethyl)-1H-imidazole hydrobromide

  • CAS No. 2939-05-1

  • Cat. No. CS-W005277
  • Purity≥95%
  • MDL No.None

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

2-(Bromomethyl)-1H-imidazole hydrobromide|CS-W005277

Structure of 2939-05-1

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General Information

  • CAS No. 2939-05-1
  • Cat. No. CS-W005277
  • Purity ≥95%
  • MDL No. None
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₄H₆Br₂N₂
  • Molecular Weight 241.91
  • Synonym(s) None
  • SMILES BrCC1=NC=CN1.Br

Description

This imidazole derivative features a bromomethyl group enabling efficient functionalization in synthetic workflows. The hydrobromide salt enhances solubility and stability under standard conditions, facilitating use in nucleophilic substitution reactions and the construction of complex heterocyclic architectures.

Application

2-(Bromomethyl)-1H-imidazole hydrobromide serves as a versatile bifunctional building block, enabling efficient installation of both imidazole and bromomethyl functionalities in a single step. Its reactive bromomethyl group facilitates nucleophilic substitution reactions, including etherification, amidation, and coupling with heterocycles, while the protonated imidazole ring enhances solubility and stability under standard synthetic conditions. The compound exhibits excellent bench stability and simplifies purification, making it ideal for modular synthesis of functionalized pharmaceutical intermediates and bioactive scaffolds.

Safety Information

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GHS Pictogram :
GHS No : GHS05,GHS07
Signal Word : Danger
UN#: 1759
Class : 8
Packing Group : Ⅱ
Hazard Statements : H302-H314
Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P304+P340-P330-P363-P405-P501

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Computational Chemistry Data

  • TPSA   28.68
  • LogP   1.8825
  • H_Acceptors   1
  • H_Donors   1
  • Rotatable_Bonds   1

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