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Atomfair N-benzyl-2-bromo-N-methylacetamide C10H12BrNO

Description N-benzyl-2-bromo-N-methylacetamide (CAS No. 336182-29-7) is a high-purity brominated acetamide derivative with the molecular formula C10H12BrNO . This compound is characterized by its benzyl and methyl substitution on the nitrogen atom, along with a reactive bromoacetamide moiety, making it a valuable intermediate in synthetic organic chemistry. Suitable for research and development applications, it is provided as a crystalline solid with ??95% purity (HPLC). Store under inert conditions at 2-8??C to maintain stability. Ideal for use in peptide coupling, nucleophilic substitution reactions, and as a precursor for pharmacologically active molecules. Available in customizable quantities with GC/MS and NMR analytical data upon…

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Description

Description

N-benzyl-2-bromo-N-methylacetamide (CAS No. 336182-29-7) is a high-purity brominated acetamide derivative with the molecular formula C10H12BrNO. This compound is characterized by its benzyl and methyl substitution on the nitrogen atom, along with a reactive bromoacetamide moiety, making it a valuable intermediate in synthetic organic chemistry. Suitable for research and development applications, it is provided as a crystalline solid with ??95% purity (HPLC). Store under inert conditions at 2-8??C to maintain stability. Ideal for use in peptide coupling, nucleophilic substitution reactions, and as a precursor for pharmacologically active molecules. Available in customizable quantities with GC/MS and NMR analytical data upon request.

  • CAS No: 336182-29-7
  • Molecular Formula: C10H12BrNO
  • Molecular Weight: 242.11
  • Exact Mass: 241.01023
  • Monoisotopic Mass: 241.01023
  • IUPAC Name: N-benzyl-2-bromo-N-methylacetamide
  • SMILES: CN(CC1=CC=CC=C1)C(=O)CBr
  • Synonyms: N-Benzyl-2-bromo-N-methylacetamide, 73391-96-5, CCRIS 1816, DTXSID30994105, DTXCID301421145

Application

N-benzyl-2-bromo-N-methylacetamide is primarily used as a versatile building block in medicinal chemistry for the synthesis of bioactive compounds. Its reactive bromoacetamide group enables selective alkylation of nucleophiles, such as amines or thiols, in drug discovery workflows. Researchers also employ it in the development of enzyme inhibitors and as a precursor for heterocyclic scaffolds. Its stability and selectivity make it suitable for controlled functionalization in complex molecular architectures.

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