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Atomfair 2-(Trifluoromethoxy)benzoyl Chloride C8H4ClF3O2

Description 2-(Trifluoromethoxy)benzoyl Chloride (CAS: 162046-61-9) is a high-purity, reactive organic compound with the molecular formula C8H4ClF3O2. This specialized benzoyl chloride derivative features a trifluoromethoxy group at the ortho position, enhancing its utility in advanced synthetic applications. Ideal for pharmaceutical intermediates, agrochemical synthesis, and material science research, this compound is rigorously tested for consistency and purity (typically ??95-98% by GC/HPLC). It is supplied in moisture-sensitive packaging under inert gas to ensure stability. Handle with care in a controlled environment due to its reactivity with nucleophiles and moisture. Available in research quantities (100mg to 10kg) with customizable bulk options.

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Description

Description

2-(Trifluoromethoxy)benzoyl Chloride (CAS: 162046-61-9) is a high-purity, reactive organic compound with the molecular formula C8H4ClF3O2. This specialized benzoyl chloride derivative features a trifluoromethoxy group at the ortho position, enhancing its utility in advanced synthetic applications. Ideal for pharmaceutical intermediates, agrochemical synthesis, and material science research, this compound is rigorously tested for consistency and purity (typically ??95-98% by GC/HPLC). It is supplied in moisture-sensitive packaging under inert gas to ensure stability. Handle with care in a controlled environment due to its reactivity with nucleophiles and moisture. Available in research quantities (100mg to 10kg) with customizable bulk options.

  • CAS No: 162046-61-9
  • Molecular Formula: C8H4ClF3O2
  • Molecular Weight: 224.56
  • Exact Mass: 223.9851915
  • Monoisotopic Mass: 223.9851915
  • IUPAC Name: 2-(trifluoromethoxy)benzoyl chloride
  • SMILES: C1=CC=C(C(=C1)C(=O)Cl)OC(F)(F)F
  • Synonyms: 2-(Trifluoromethoxy)benzoyl Chloride, 162046-61-9, DTXSID60380431, DTXCID50331457, 642-457-4

Application

2-(Trifluoromethoxy)benzoyl Chloride serves as a key building block in the synthesis of fluorinated pharmaceuticals, particularly for introducing the trifluoromethoxybenzoyl moiety into target molecules. It is employed in peptide coupling reactions and as an intermediate for herbicides and fungicides in agrochemical research. The compound’s electron-withdrawing properties make it valuable in materials science for modifying polymer backbones or creating specialty coatings.

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