Atomfair 1-(4-(Trifluoromethoxy)phenyl)ethan-1-one C9H7F3O2

Description 1-(4-(Trifluoromethoxy)phenyl)ethan-1-one (CAS No. 85013-98-5) is a high-purity organic compound with the molecular formula C9H7F3O2. This trifluoromethoxy-substituted acetophenone derivative is a valuable building block in synthetic organic chemistry, particularly in pharmaceutical and agrochemical research. The presence of the trifluoromethoxy group enhances the compound’s lipophilicity and metabolic stability, making it an attractive intermediate for drug discovery. Our product is rigorously tested to ensure ??98% purity (HPLC/GC) and is supplied as a crystalline solid with consistent batch-to-batch quality. Suitable for use in nucleophilic additions, Friedel-Crafts reactions, and as a precursor for heterocyclic synthesis. Store in a cool, dry place protected from light.

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Description

Description

1-(4-(Trifluoromethoxy)phenyl)ethan-1-one (CAS No. 85013-98-5) is a high-purity organic compound with the molecular formula C9H7F3O2. This trifluoromethoxy-substituted acetophenone derivative is a valuable building block in synthetic organic chemistry, particularly in pharmaceutical and agrochemical research. The presence of the trifluoromethoxy group enhances the compound’s lipophilicity and metabolic stability, making it an attractive intermediate for drug discovery. Our product is rigorously tested to ensure ??98% purity (HPLC/GC) and is supplied as a crystalline solid with consistent batch-to-batch quality. Suitable for use in nucleophilic additions, Friedel-Crafts reactions, and as a precursor for heterocyclic synthesis. Store in a cool, dry place protected from light.

  • CAS No: 85013-98-5
  • Molecular Formula: C9H7F3O2
  • Molecular Weight: 204.15
  • Exact Mass: 204.03981395
  • Monoisotopic Mass: 204.03981395
  • IUPAC Name: 1-[4-(trifluoromethoxy)phenyl]ethanone
  • SMILES: CC(=O)C1=CC=C(C=C1)OC(F)(F)F
  • Synonyms: 4′-(Trifluoromethoxy)acetophenone, 1-(4-(trifluoromethoxy)phenyl)ethanone, 1-[4-(trifluoromethoxy)phenyl]ethanone, 1-[4-(trifluoromethoxy)phenyl]ethan-1-one, 1-(4-(Trifluoromethoxy)phenyl)ethan-1-one

Application

This compound serves as a key intermediate in the synthesis of biologically active molecules, particularly in the development of pharmaceuticals targeting CNS disorders. The trifluoromethoxy group imparts improved blood-brain barrier penetration, making it valuable for neuroactive compound development. Researchers utilize it in Suzuki coupling reactions to create novel aryl ketone derivatives. It’s also employed in the synthesis of liquid crystal materials and as a building block for agricultural chemicals.

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