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LAUREN-1-ENE
SpectraBase Compound ID DLYHiG2dwqp
InChI InChI=1S/C20H32/c1-14-7-6-10-18(4)12-9-16-17(2,3)13-19(5)11-8-15(14)20(16,18)19/h8,14,16H,6-7,9-13H2,1-5H3/t14-,16-,18+,19-,20?/m1/s1
InChIKey TYDFDHZTDWVUJF-IAAPBBNJSA-N
Mol Weight 272.5 g/mol
Molecular Formula C20H32
Exact Mass 272.250401 g/mol
Enantiomer InChIKey TYDFDHZTDWVUJF-UJSRRMEDSA-N
Copyright Database Compilation Copyright © 2023-2024 John Wiley and Sons, Inc. Copyright © 2023-2024 John Wiley and Sons, Inc., Portions Copyright Wiley-VCH GmbH, Adams Library under license from Diablo Analytical. All Rights Reserved.
Source of Spectrum Adams' Essential Oil Components (GC-MS), Version 4
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum Adams' Essential Oil Components (GC-MS), Version 4
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 © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • Laurenene
Title Journal or Book Year
The Chemistry of Laurenene. XVI. Investigation of the Mechanism of a Cationic Rearrangement Australian Journal of Chemistry 1993
The Chemistry of Laurenene. VIII. Laurena-1(15),2-diene, Laurena-1,14-diene and Lauren-1(15)-ene Australian Journal of Chemistry 1988
The chemistry of lauren-l-ene. II. Remote functionalization reactions of the laurenan-2-ols and the 1bH-laurenan-2-ols Australian Journal of Chemistry 1980
The chemistry of lauren-1-ene. I. Nuclear magnetic resonance spectra and the course of osmic acid oxidation Australian Journal of Chemistry 1980

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