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Atomfair 1,1′-(2,7-Naphthalenediyl) bis(1,1,1-trifluoromethanesulfonate) C12H6F6O6S2

Description 1,1′-(2,7-Naphthalenediyl) bis(1,1,1-trifluoromethanesulfonate) (CAS No. 151391-00-3) is a high-purity, specialized organic compound with the molecular formula C12H6F6O6S2. This bifunctional triflate derivative features a naphthalene core symmetrically substituted with two trifluoromethanesulfonate (triflate) groups at the 2- and 7-positions, making it an excellent electrophilic reagent for advanced organic synthesis and cross-coupling reactions. Its IUPAC name is [7-(trifluoromethylsulfonyloxy)naphthalen-2-yl] trifluoromethanesulfonate . The compound is supplied as a crystalline solid with exceptional stability under inert conditions, ensuring reliable performance in sensitive applications. Ideal for researchers in pharmaceuticals, materials science, and catalysis, this product undergoes rigorous QC testing (HPLC, NMR) to guarantee ??98% purity. Store in…

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Description

Description

1,1′-(2,7-Naphthalenediyl) bis(1,1,1-trifluoromethanesulfonate) (CAS No. 151391-00-3) is a high-purity, specialized organic compound with the molecular formula C12H6F6O6S2. This bifunctional triflate derivative features a naphthalene core symmetrically substituted with two trifluoromethanesulfonate (triflate) groups at the 2- and 7-positions, making it an excellent electrophilic reagent for advanced organic synthesis and cross-coupling reactions. Its IUPAC name is [7-(trifluoromethylsulfonyloxy)naphthalen-2-yl] trifluoromethanesulfonate. The compound is supplied as a crystalline solid with exceptional stability under inert conditions, ensuring reliable performance in sensitive applications. Ideal for researchers in pharmaceuticals, materials science, and catalysis, this product undergoes rigorous QC testing (HPLC, NMR) to guarantee ??98% purity. Store in a cool, dry place under argon to maintain reactivity.

  • CAS No: 151391-00-3
  • Molecular Formula: C12H6F6O6S2
  • Molecular Weight: 424.3
  • Exact Mass: 423.95099923
  • Monoisotopic Mass: 423.95099923
  • IUPAC Name: [7-(trifluoromethylsulfonyloxy)naphthalen-2-yl] trifluoromethanesulfonate
  • SMILES: C1=CC(=CC2=C1C=CC(=C2)OS(=O)(=O)C(F)(F)F)OS(=O)(=O)C(F)(F)F
  • Synonyms: 151391-00-3, 2,7-Naphthalenebis(trifluoromethanesulfonate), DTXSID701174194, DTXCID301605581, 1,1′-(2,7-Naphthalenediyl) bis(1,1,1-trifluoromethanesulfonate)

Application

This compound serves as a versatile building block in palladium-catalyzed cross-coupling reactions (e.g., Suzuki, Heck) due to its highly reactive triflate leaving groups. It enables the synthesis of extended ??-conjugated systems for organic electronics such as OLEDs and OFETs. The naphthalene backbone facilitates rigid, planar architectures in polymer and small-molecule semiconductors. Researchers also employ it to create fluorescent probes and ligands for metal-organic frameworks (MOFs).

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