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Atomfair 2-(Trifluoromethoxy)anisole C8H7F3O2

Description 2-(Trifluoromethoxy)anisole (CAS No. 261952-22-1) is a high-purity fluorinated aromatic compound with the molecular formula C8H7F3O2. This specialty chemical, also known by its IUPAC name 1-methoxy-2-(trifluoromethoxy)benzene , is a versatile building block in organic synthesis and pharmaceutical research. Its unique trifluoromethoxy and methoxy substituents make it valuable for modulating lipophilicity and electronic properties in drug discovery. Available in >98% purity (GC), this compound is supplied in rigorously tested batches with full analytical documentation (GC/MS, NMR) to ensure reproducibility. Suitable for use in Suzuki couplings, nucleophilic substitutions, and other transformations, it is packaged under inert gas in amber glass vials to…

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Description

Description

2-(Trifluoromethoxy)anisole (CAS No. 261952-22-1) is a high-purity fluorinated aromatic compound with the molecular formula C8H7F3O2. This specialty chemical, also known by its IUPAC name 1-methoxy-2-(trifluoromethoxy)benzene, is a versatile building block in organic synthesis and pharmaceutical research. Its unique trifluoromethoxy and methoxy substituents make it valuable for modulating lipophilicity and electronic properties in drug discovery. Available in >98% purity (GC), this compound is supplied in rigorously tested batches with full analytical documentation (GC/MS, NMR) to ensure reproducibility. Suitable for use in Suzuki couplings, nucleophilic substitutions, and other transformations, it is packaged under inert gas in amber glass vials to ensure stability.

  • CAS No: 261952-22-1
  • Molecular Formula: C8H7F3O2
  • Molecular Weight: 192.13
  • Exact Mass: 192.03981395
  • Monoisotopic Mass: 192.03981395
  • IUPAC Name: 1-methoxy-2-(trifluoromethoxy)benzene
  • SMILES: COC1=CC=CC=C1OC(F)(F)F
  • Synonyms: 2-(Trifluoromethoxy)anisole, 261952-22-1, DTXSID10380406, DTXCID50331432, 687-921-7

Application

2-(Trifluoromethoxy)anisole serves as a key intermediate in the synthesis of bioactive molecules, particularly in the development of CNS-active pharmaceuticals where the trifluoromethoxy group enhances blood-brain barrier penetration. It is employed in material science for creating fluorinated liquid crystals and dielectric materials. Researchers also utilize this compound as a probe for studying electronic effects of simultaneous alkoxy/fluoroalkoxy substitution on aromatic systems.

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