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Manoyloxide
SpectraBase Compound ID Jjb8tL9UdMt
InChI InChI=1S/C20H34O/c1-7-18(4)13-9-16-19(5)12-8-11-17(2,3)15(19)10-14-20(16,6)21-18/h7,15-16H,1,8-14H2,2-6H3/t15-,16+,18-,19-,20+/m0/s1
InChIKey IGGWKHQYMAJOHK-HHUCQEJWSA-N
Mol Weight 290.5 g/mol
Molecular Formula C20H34O
Exact Mass 290.260966 g/mol
Enantiomer InChIKey IGGWKHQYMAJOHK-LHDHZVESSA-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 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 FF-7-142-4 (DOI: 10.1002/ffj.2730070308)
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum QA-34-222-8
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum FF-7-142-4
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 Unknown
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • MANOYL-OXIDE;8,13-EPOXYLABD-14-ENE
  • (+)-Manoyl oxide
  • Manool oxide
  • (3R,4aR,6aS,10aS,10bR)-3,4a,7,7,10a-pentamethyl-3-vinyldodecahydro-1H-benzo[f]chromene
Title Journal or Book Year
Chelodane, Barekoxide, and Zaatirin--Three New Diterpenoids from the Marine Sponge Chelonaplysilla erecta Journal of Natural Products 1992
Microbial transformation of manool and (12Z)-labda-8(17),12,14-triene by Rhodococcus erythropolis JTS-131. Agricultural and Biological Chemistry 1983
13C-NMR. Spectroscopy of Naturally Occurring Substances. XXXV. Labdanic diterpenes Helvetica Chimica Acta 1975
Carbon-13 NMR Studies of Labdane Diterpenoids. Acta Chemica Scandinavica 1975

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