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Atomfair N-(2-Bromo-4,5-difluorophenyl)acetamide C8H6BrF2NO

Description N-(2-Bromo-4,5-difluorophenyl)acetamide (CAS No. 64695-81-4) is a high-purity halogenated acetamide derivative with the molecular formula C8H6BrF2NO . This compound features a bromo- and difluoro-substituted phenyl ring coupled to an acetamide functional group, making it a valuable intermediate in organic synthesis and pharmaceutical research. With a molecular weight of 250.04 g/mol, it is supplied as a crystalline solid with >95% purity (HPLC) and is rigorously tested for consistency. Ideal for cross-coupling reactions, Suzuki-Miyaura couplings, and as a precursor for bioactive molecule development. Store in a cool, dry place under inert conditions to ensure stability.

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Description

Description

N-(2-Bromo-4,5-difluorophenyl)acetamide (CAS No. 64695-81-4) is a high-purity halogenated acetamide derivative with the molecular formula C8H6BrF2NO. This compound features a bromo- and difluoro-substituted phenyl ring coupled to an acetamide functional group, making it a valuable intermediate in organic synthesis and pharmaceutical research. With a molecular weight of 250.04 g/mol, it is supplied as a crystalline solid with >95% purity (HPLC) and is rigorously tested for consistency. Ideal for cross-coupling reactions, Suzuki-Miyaura couplings, and as a precursor for bioactive molecule development. Store in a cool, dry place under inert conditions to ensure stability.

  • CAS No: 64695-81-4
  • Molecular Formula: C8H6BrF2NO
  • Molecular Weight: 250.04
  • Exact Mass: 248.96008
  • Monoisotopic Mass: 248.96008
  • IUPAC Name: N-(2-bromo-4,5-difluorophenyl)acetamide
  • SMILES: CC(=O)NC1=CC(=C(C=C1Br)F)F
  • Synonyms: N-(2-BROMO-4,5-DIFLUOROPHENYL)ACETAMIDE, 64695-81-4, MFCD08705814, Acetamide, N-(2-bromo-4,5-difluorophenyl)-, DTXSID20525902

Application

N-(2-Bromo-4,5-difluorophenyl)acetamide serves as a versatile building block in medicinal chemistry, particularly in the synthesis of fluorinated drug candidates targeting CNS disorders. Its bromo and difluoro substituents enhance electrophilic reactivity for palladium-catalyzed cross-coupling reactions. Researchers also utilize it to develop agrochemicals and advanced materials with tailored electronic properties. The compound’s stability under acidic conditions makes it suitable for multi-step synthetic workflows.

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