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CAMPHANE-2-EXO,3-EXO-DIOL
SpectraBase Compound ID ApirHOZj7eC
InChI InChI=1S/C10H18O2/c1-9(2)6-4-5-10(9,3)8(12)7(6)11/h6-8,11-12H,4-5H2,1-3H3/t6-,7-,8-,10+/m0/s1
InChIKey AYEOSGBMQHXVER-AZQAYCESSA-N
Mol Weight 170.25 g/mol
Molecular Formula C10H18O2
Exact Mass 170.13068 g/mol
Enantiomer InChIKey AYEOSGBMQHXVER-DQUBFYRCSA-N
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent CDCL3
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum I-57-739-0
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum KC-0-779-4
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum KC-0-779-3
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum KC-0-779-2
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
  • BORNANE-2-EXO-3-EXO-DIOL
  • (+)-2-EXO-3-EXO-CAMPHANE-2,3-DIOL
  • 2-exo-3-exo-Camphane-2,3-diol
  • Bicyclo[2.2.1]heptane-2,3-diol, 1,7,7-trimethyl-, [1S-(2-endo,3-exo)]-
  • 2,3-Bornanediol
  • BICYCLO[2.2.1]HEPTAN-2,3-DIOL, 1,7,7-TRIMETHYL-
Title Journal or Book Year
Biotransformation of (+)- and (−)-camphorquinones to camphanediols by Glomerella cingulata Phytochemistry 1997
Synthesis of camphor based chiral crown ethers and their interactions with amino acid derivatives Journal of the Chemical Society, Perkin Transactions 2 1995
The configurations of the trans-Camphane-2,3-diols Australian Journal of Chemistry 1984

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