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CS-W001157 4
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5-(Bromomethyl)-1-methyl-4-nitro-1H-imidazole

  • CAS No. 1017279-02-5

  • Cat. No. CS-0083003
  • Molecule weight220.02
  • Purity≥97%
  • MDL No.None

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

5-(Bromomethyl)-1-methyl-4-nitro-1H-imidazole|CS-0083003

Structure of 1017279-02-5

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General Information

  • CAS No. 1017279-02-5
  • Cat. No. CS-0083003
  • Purity ≥97%
  • MDL No. None
  • Storage -20°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₅H₆BrN₃O₂
  • Molecular Weight 220.02
  • Synonym(s) None
  • SMILES CN1C=NC([N+]([O-])=O)=C1CBr

Description

This bromomethyl-substituted imidazole delivers a reactive handle for nucleophilic functionalization, combining a methylated core with a para-nitro group that enhances electrophilicity. The bromomethyl moiety enables efficient coupling reactions under mild conditions, offering reliable access to complex heterocyclic architectures in synthetic and medicinal chemistry workflows.

Application

5-(Bromomethyl)-1-methyl-4-nitro-1H-imidazole serves as a versatile bifunctional building block for the synthesis of imidazole-based scaffolds. The bromomethyl group enables efficient nucleophilic substitution reactions, while the nitro and methyl substituents provide electronic modulation and enhanced stability. This compound facilitates the construction of pharmaceutically relevant heterocycles and supports downstream functionalization in medicinal chemistry workflows.

Safety Information

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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-P330-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   60.96
  • LogP   1.2232
  • H_Acceptors   4
  • H_Donors   0
  • Rotatable_Bonds   2

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