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Atomfair (S)-Methyl Oxazaborolidine C18H20BNO

Description (S)-Methyl Oxazaborolidine (CAS: 112022-81-8) is a highly specialized chiral oxazaborolidine derivative with the molecular formula C18H20BNO. This compound, also known by its IUPAC name 1-methyl-3,3-diphenyl-3a,4,5,6-tetrahydropyrrolo[1,2-c][1,3,2]oxazaborole , is a valuable boron-containing heterocycle widely utilized in asymmetric synthesis and catalytic applications. Its rigid, enantiopure structure makes it an efficient chiral auxiliary or catalyst in organic transformations, particularly in enantioselective reductions and cycloadditions. The compound is supplied as a high-purity solid, rigorously characterized by NMR, HPLC, and elemental analysis to ensure consistency for research and industrial use. Store under inert conditions to maintain stability.

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Description

Description

(S)-Methyl Oxazaborolidine (CAS: 112022-81-8) is a highly specialized chiral oxazaborolidine derivative with the molecular formula C18H20BNO. This compound, also known by its IUPAC name 1-methyl-3,3-diphenyl-3a,4,5,6-tetrahydropyrrolo[1,2-c][1,3,2]oxazaborole, is a valuable boron-containing heterocycle widely utilized in asymmetric synthesis and catalytic applications. Its rigid, enantiopure structure makes it an efficient chiral auxiliary or catalyst in organic transformations, particularly in enantioselective reductions and cycloadditions. The compound is supplied as a high-purity solid, rigorously characterized by NMR, HPLC, and elemental analysis to ensure consistency for research and industrial use. Store under inert conditions to maintain stability.

  • CAS No: 112022-81-8
  • Molecular Formula: C18H20BNO
  • Molecular Weight: 277.2
  • Exact Mass: 277.1637944
  • Monoisotopic Mass: 277.1637944
  • IUPAC Name: 1-methyl-3,3-diphenyl-3a,4,5,6-tetrahydropyrrolo[1,2-c][1,3,2]oxazaborole
  • SMILES: B1(N2CCCC2C(O1)(C3=CC=CC=C3)C4=CC=CC=C4)C
  • Synonyms: 133261-83-3, (S)-Methyl Oxazaborolidine, 1-methyl-3,3-diphenyl-3a,4,5,6-tetrahydropyrrolo[1,2-c][1,3,2]oxazaborole, tetrahydro-1-methyl-3,3-diphenyl-1h,3h-pyrrolo[1,2-c][1,3,2]oxazaborole, 1-methyl-3,3-diphenyl-hexahydropyrrolo[1,2-c][1,3,2]oxazaborole

Application

(S)-Methyl Oxazaborolidine is primarily employed as a chiral catalyst in asymmetric synthesis, enabling high enantioselectivity in ketone and imine reductions. It is also used in Diels-Alder reactions and other cycloadditions to induce stereochemical control. Researchers value this compound for its ability to produce enantiomerically enriched intermediates in pharmaceutical and fine chemical synthesis.

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