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Atomfair 2,3-Pinanediol C10H18O2

Description 2,3-Pinanediol (CAS No. 18680-27-8) is a high-purity bicyclic diol compound with the molecular formula C10H18O2and IUPAC name 2,6,6-trimethylbicyclo[3.1.1]heptane-2,3-diol. This chiral building block is derived from pinene and features two hydroxyl groups at the 2- and 3-positions of the pinane skeleton, offering unique stereochemical properties for asymmetric synthesis. Our product is rigorously tested to meet the highest standards of purity and consistency, making it ideal for pharmaceutical intermediates, fragrance synthesis, and chiral resolution studies. Available in various enantiomeric forms to suit specific research needs, 2,3-Pinanediol is supplied with comprehensive analytical documentation including GC/HPLC purity reports and structural verification data.

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Description

Description

2,3-Pinanediol (CAS No. 18680-27-8) is a high-purity bicyclic diol compound with the molecular formula C10H18O2 and IUPAC name 2,6,6-trimethylbicyclo[3.1.1]heptane-2,3-diol. This chiral building block is derived from pinene and features two hydroxyl groups at the 2- and 3-positions of the pinane skeleton, offering unique stereochemical properties for asymmetric synthesis. Our product is rigorously tested to meet the highest standards of purity and consistency, making it ideal for pharmaceutical intermediates, fragrance synthesis, and chiral resolution studies. Available in various enantiomeric forms to suit specific research needs, 2,3-Pinanediol is supplied with comprehensive analytical documentation including GC/HPLC purity reports and structural verification data.

  • CAS No: 18680-27-8
  • Molecular Formula: C10H18O2
  • Molecular Weight: 170.25
  • Exact Mass: 170.130679813
  • Monoisotopic Mass: 170.130679813
  • IUPAC Name: 2,6,6-trimethylbicyclo[3.1.1]heptane-2,3-diol
  • SMILES: CC1(C2CC1C(C(C2)O)(C)O)C
  • Synonyms: 2,3-Pinanediol, 53404-49-2, 2,6,6-Trimethylbicyclo[3.1.1]heptane-2,3-diol, Caswell No. 442, UNII-0YBA7G0JSH

Application

2,3-Pinanediol serves as a versatile chiral auxiliary in asymmetric organic synthesis, particularly for the preparation of stereoselective catalysts and ligands. The compound finds application in the development of fragrance ingredients due to its rigid bicyclic structure and hydroxyl functionality. Researchers also utilize 2,3-Pinanediol as a starting material for the synthesis of biologically active compounds and as a resolving agent for racemic mixtures in chromatography applications.

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