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Atomfair 2,2′-Dibromo-6,6′-difluoro-1,1′-biphenyl C12H6Br2F2

Description 2,2′-Dibromo-6,6′-difluoro-1,1′-biphenyl (CAS No. 1316276-94-4) is a high-purity halogenated biphenyl compound with the molecular formula C12H6Br2F2. This specialized aromatic compound features two bromine and two fluorine substituents at the 2,2′ and 6,6′ positions, respectively, creating a sterically hindered and electron-deficient biphenyl system. With a molecular weight of 323.98 g/mol, this compound is particularly valuable in advanced organic synthesis, serving as a key intermediate for the preparation of functionalized materials, ligands, and pharmaceutical building blocks. The compound is supplied as a crystalline solid with ??95% purity (HPLC) and is rigorously tested for consistency in quality and performance. Proper storage at 2-8??C…

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Description

Description

2,2′-Dibromo-6,6′-difluoro-1,1′-biphenyl (CAS No. 1316276-94-4) is a high-purity halogenated biphenyl compound with the molecular formula C12H6Br2F2. This specialized aromatic compound features two bromine and two fluorine substituents at the 2,2′ and 6,6′ positions, respectively, creating a sterically hindered and electron-deficient biphenyl system. With a molecular weight of 323.98 g/mol, this compound is particularly valuable in advanced organic synthesis, serving as a key intermediate for the preparation of functionalized materials, ligands, and pharmaceutical building blocks. The compound is supplied as a crystalline solid with ??95% purity (HPLC) and is rigorously tested for consistency in quality and performance. Proper storage at 2-8??C under inert atmosphere is recommended to maintain stability.

  • CAS No: 1316276-94-4
  • Molecular Formula: C12H6Br2F2
  • Molecular Weight: 347.98
  • Exact Mass: 347.87838
  • Monoisotopic Mass: 345.88043
  • IUPAC Name: 1-bromo-2-(2-bromo-6-fluorophenyl)-3-fluorobenzene
  • SMILES: C1=CC(=C(C(=C1)Br)C2=C(C=CC=C2Br)F)F
  • Synonyms: 2,2′-Dibromo-6,6′-difluoro-1,1′-biphenyl, 1316276-94-4, G67627

Application

2,2′-Dibromo-6,6′-difluoro-1,1′-biphenyl serves as a versatile building block in the synthesis of advanced organic materials, particularly in the development of fluorinated liquid crystals and OLED intermediates. Its electron-withdrawing properties make it valuable for constructing ??-conjugated systems in organic electronics. Researchers also utilize this compound as a precursor for palladium-catalyzed cross-coupling reactions to create complex biaryl structures for pharmaceutical applications.

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