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Atomfair (S)-(+)-1,1′-Bi-2-naphthol bis(trifluoromethanesulfonate) C22H12F6O6S2

Description (S)-(+)-1,1′-Bi-2-naphthol bis(trifluoromethanesulfonate) (CAS No. 126613-06-7) is a highly specialized chiral reagent with the molecular formula C22H12F6O6S2. This enantiomerically pure compound is derived from (S)-(+)-1,1′-Bi-2-naphthol (BINOL) and features two trifluoromethanesulfonate (triflate) groups, making it an excellent chiral catalyst or auxiliary in asymmetric synthesis. Its rigid binaphthyl backbone ensures high stereoselectivity, while the triflate groups serve as excellent leaving groups for nucleophilic substitution reactions. This compound is widely utilized in organic synthesis, pharmaceuticals, and materials science due to its ability to induce chirality in complex molecular frameworks. Packaged under inert conditions to ensure stability and purity, it is ideal for researchers…

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Description

Description

(S)-(+)-1,1′-Bi-2-naphthol bis(trifluoromethanesulfonate) (CAS No. 126613-06-7) is a highly specialized chiral reagent with the molecular formula C22H12F6O6S2. This enantiomerically pure compound is derived from (S)-(+)-1,1′-Bi-2-naphthol (BINOL) and features two trifluoromethanesulfonate (triflate) groups, making it an excellent chiral catalyst or auxiliary in asymmetric synthesis. Its rigid binaphthyl backbone ensures high stereoselectivity, while the triflate groups serve as excellent leaving groups for nucleophilic substitution reactions. This compound is widely utilized in organic synthesis, pharmaceuticals, and materials science due to its ability to induce chirality in complex molecular frameworks. Packaged under inert conditions to ensure stability and purity, it is ideal for researchers requiring precise enantiomeric control.

  • CAS No: 126613-06-7
  • Molecular Formula: C22H12F6O6S2
  • Molecular Weight: 550.5
  • Exact Mass: 549.99794942
  • Monoisotopic Mass: 549.99794942
  • IUPAC Name: [1-[2-(trifluoromethylsulfonyloxy)naphthalen-1-yl]naphthalen-2-yl] trifluoromethanesulfonate
  • SMILES: C1=CC=C2C(=C1)C=CC(=C2C3=C(C=CC4=CC=CC=C43)OS(=O)(=O)C(F)(F)F)OS(=O)(=O)C(F)(F)F
  • Synonyms: (S)-(+)-1,1′-Bi-2-naphthol bis(trifluoromethanesulfonate), 1,1′-Bi-2-naphthol bis(trifluoromethanesulfonate), 2,2′-bis(trifluoromethanesulfonyloxy)-1,1′-binaphthyl, 603-279-2, 603-283-4

Application

This compound is extensively used as a chiral catalyst or ligand in asymmetric synthesis, particularly in C-C bond-forming reactions. It is valuable in pharmaceutical research for the synthesis of enantiomerically pure drugs and intermediates. Additionally, it serves as a precursor for chiral polymers and advanced materials requiring optical activity.

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