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Atomfair 3′-Chloro-4′-fluoroacetophenone C8H6ClFO

Description 3′-Chloro-4′-fluoroacetophenone (CAS No. 2923-66-2) is a high-purity organic compound with the molecular formula C8H6ClFO. Also known as 1-(3-chloro-4-fluorophenyl)ethanone, this aromatic ketone features a chloro- and fluoro-substituted phenyl ring, making it a versatile intermediate in pharmaceutical and agrochemical synthesis. Its well-defined structure (molecular weight: 172.58 g/mol) ensures consistent reactivity, ideal for nucleophilic substitutions, condensations, and other fine chemical transformations. This product is rigorously tested for purity (typically ??98% by GC or HPLC) and is supplied as a crystalline solid with excellent shelf stability under recommended storage conditions (2-8??C, inert atmosphere). Suitable for research, process development, and scale-up applications.

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Description

Description

3′-Chloro-4′-fluoroacetophenone (CAS No. 2923-66-2) is a high-purity organic compound with the molecular formula C8H6ClFO. Also known as 1-(3-chloro-4-fluorophenyl)ethanone, this aromatic ketone features a chloro- and fluoro-substituted phenyl ring, making it a versatile intermediate in pharmaceutical and agrochemical synthesis. Its well-defined structure (molecular weight: 172.58 g/mol) ensures consistent reactivity, ideal for nucleophilic substitutions, condensations, and other fine chemical transformations. This product is rigorously tested for purity (typically ??98% by GC or HPLC) and is supplied as a crystalline solid with excellent shelf stability under recommended storage conditions (2-8??C, inert atmosphere). Suitable for research, process development, and scale-up applications.

  • CAS No: 2923-66-2
  • Molecular Formula: C8H6ClFO
  • Molecular Weight: 172.58
  • Exact Mass: 172.0091207
  • Monoisotopic Mass: 172.0091207
  • IUPAC Name: 1-(3-chloro-4-fluorophenyl)ethanone
  • SMILES: CC(=O)C1=CC(=C(C=C1)F)Cl
  • Synonyms: 3′-Chloro-4′-fluoroacetophenone, 2923-66-2, 1-(3-Chloro-4-fluorophenyl)ethanone, DTXSID70334344, DTXCID80285434

Application

3′-Chloro-4′-fluoroacetophenone serves as a key building block in the synthesis of bioactive molecules, particularly in the development of pharmaceuticals targeting CNS disorders and antimicrobial agents. Its halogenated structure facilitates further functionalization via Suzuki couplings or nucleophilic aromatic substitutions. Researchers also utilize it in material science for designing liquid crystals and photoactive compounds. The compound’s reactivity is exploited in combinatorial chemistry for library generation.

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