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Atomfair 2′-Bromo-4′-(trifluoromethoxy)acetanilide C9H7BrF3NO2

Description 2′-Bromo-4′-(trifluoromethoxy)acetanilide (CAS No. 131395-29-4) is a high-purity organic compound with the molecular formula C9H7BrF3NO2and IUPAC name N-[2-bromo-4-(trifluoromethoxy)phenyl]acetamide . This specialized chemical features a bromo-substituted phenyl ring and a trifluoromethoxy group, making it a valuable intermediate for pharmaceutical and agrochemical research. Its unique structure enables applications in cross-coupling reactions, medicinal chemistry, and material science. Available in >98% purity (HPLC), this compound is supplied in sealed packaging under inert conditions to ensure stability. Ideal for researchers seeking halogenated anilide derivatives with enhanced reactivity.

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Description

Description

2′-Bromo-4′-(trifluoromethoxy)acetanilide (CAS No. 131395-29-4) is a high-purity organic compound with the molecular formula C9H7BrF3NO2 and IUPAC name N-[2-bromo-4-(trifluoromethoxy)phenyl]acetamide. This specialized chemical features a bromo-substituted phenyl ring and a trifluoromethoxy group, making it a valuable intermediate for pharmaceutical and agrochemical research. Its unique structure enables applications in cross-coupling reactions, medicinal chemistry, and material science. Available in >98% purity (HPLC), this compound is supplied in sealed packaging under inert conditions to ensure stability. Ideal for researchers seeking halogenated anilide derivatives with enhanced reactivity.

  • CAS No: 131395-29-4
  • Molecular Formula: C9H7BrF3NO2
  • Molecular Weight: 298.06
  • Exact Mass: 296.96123
  • Monoisotopic Mass: 296.96123
  • IUPAC Name: N-[2-bromo-4-(trifluoromethoxy)phenyl]acetamide
  • SMILES: CC(=O)NC1=C(C=C(C=C1)OC(F)(F)F)Br
  • Synonyms: 131395-29-4, 2′-Bromo-4′-(trifluoromethoxy)acetanilide, DTXSID90372384, DTXCID30323416, N-(2-Bromo-4-(trifluoromethoxy)phenyl)acetamide

Application

2′-Bromo-4′-(trifluoromethoxy)acetanilide serves as a key building block in Suzuki-Miyaura and Buchwald-Hartwig coupling reactions for drug discovery. The trifluoromethoxy group enhances metabolic stability in bioactive molecules, making it valuable for medicinal chemistry optimization. Researchers also utilize this compound in the synthesis of liquid crystals and advanced materials due to its halogenated aromatic core.

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