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Atomfair 2-Bromo-5-(trifluoromethoxy)phenol C7H4BrF3O2

Description 2-Bromo-5-(trifluoromethoxy)phenol (CAS No. 205371-26-2) is a high-purity halogenated phenolic compound with the molecular formula C7H4BrF3O2. This specialized chemical features a bromine substituent and a trifluoromethoxy group on the phenol ring, making it a valuable intermediate for advanced organic synthesis and pharmaceutical research. Its unique structure enhances reactivity in electrophilic aromatic substitution and coupling reactions. Available in >98% purity (HPLC), this compound is supplied in rigorously tested vials under inert atmosphere to ensure stability. Ideal for medicinal chemistry, agrochemical development, and material science applications requiring precise fluorinated building blocks. Store at 2-8??C in a dry, dark environment.

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Description

Description

2-Bromo-5-(trifluoromethoxy)phenol (CAS No. 205371-26-2) is a high-purity halogenated phenolic compound with the molecular formula C7H4BrF3O2. This specialized chemical features a bromine substituent and a trifluoromethoxy group on the phenol ring, making it a valuable intermediate for advanced organic synthesis and pharmaceutical research. Its unique structure enhances reactivity in electrophilic aromatic substitution and coupling reactions. Available in >98% purity (HPLC), this compound is supplied in rigorously tested vials under inert atmosphere to ensure stability. Ideal for medicinal chemistry, agrochemical development, and material science applications requiring precise fluorinated building blocks. Store at 2-8??C in a dry, dark environment.

  • CAS No: 205371-26-2
  • Molecular Formula: C7H4BrF3O2
  • Molecular Weight: 257.00
  • Exact Mass: 255.93468
  • Monoisotopic Mass: 255.93468
  • IUPAC Name: 2-bromo-5-(trifluoromethoxy)phenol
  • SMILES: C1=CC(=C(C=C1OC(F)(F)F)O)Br
  • Synonyms: 2-Bromo-5-(trifluoromethoxy)phenol, 205371-26-2, RHRRKORKKIVAGJ-UHFFFAOYSA-, DTXSID60590674, DTXCID50541438

Application

2-Bromo-5-(trifluoromethoxy)phenol serves as a key precursor in the synthesis of trifluoromethoxy-containing pharmaceuticals and agrochemicals. Its electron-withdrawing groups facilitate Suzuki-Miyaura cross-coupling reactions for biaryl compound production. Researchers utilize this compound to develop PET radiotracers due to the metabolically stable trifluoromethoxy moiety. In material science, it acts as a monomer for flame-retardant polymers.

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