17-ACETOXY-8,13-EPOXY-14,15-DINORLABDAN-13-XI-OL
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 6WLnucHK0bI |
|---|---|
| InChI | InChI=1S/C20H34O4/c1-14(21)23-13-20-12-8-15-17(2,3)9-6-10-18(15,4)16(20)7-11-19(5,22)24-20/h15-16,22H,6-13H2,1-5H3/t15?,16?,18-,19?,20-/m0/s1 |
| InChIKey | QBSANUFFVFPNAS-MUEWKZGQSA-N |
| Mol Weight | 338.5 g/mol |
| Molecular Formula | C20H34O4 |
| Exact Mass | 338.24571 g/mol |
| Enantiomer InChIKey | QBSANUFFVFPNAS-SEPGVAQZSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
19-ACETOXYMANOYL OXIDE
1H-NAPHTHO[2,1-B]PYRAN-3,7-DIMETHANOL, 3-ETHENYLDODECAHYDRO-4A,7,10A-TRIMETHYL-7-ACETATE
2H-3,5a-Epoxynaphth[2,1-b]oxepin, dodecahydro-3,8,8,11a-tetramethyl-, [3R-(3.alpha.,5a.alpha.,7a.beta.,11a.alpha.,11b.beta.)]-
(5aS,7aS,11aS,11bS)-3,8,8,11a-tetramethyldodecahydro-3H-3,5a-epoxynaphtho[1,2-c]oxepine
TARAPACOL-DIACETATE;14,15-DIACETOXY-13-EPI-MANOYLOXIDE
14,15,19-TRIHYDROXY-13-EPI-ENT-MANOYLOXIDE
ENT-16-HYDROXY-14E-15E-EPOXY-13-EPI-MANOYL OXIDE
ENT-16-HYDROXY-14-XI,15-XI-EPOXY-13-EPI-MANOYL-OXIDE
5H-3,5a-Epoxynaphth[2,1-c]oxepin, dodecahydro-3,8,8,11a-tetramethyl-, [3S-(3.alpha.,5a.alpha.,7a.beta.,11a.alpha.,11b.beta.)]-
5H-3,5a-Epoxynaphth[2,1-c]oxepin, dodecahydro-3,8,8,11a-tetramethyl-, [3R-(3.alpha.,5a.alpha.,7a.alpha.,11a.beta.,11b.alpha.)]-
| Title | Journal or Book | Year |
|---|---|---|
| Rin -Opening of Acetal III (8,13/13,17-Diepoxy-14,15-dinorlabdane) and the Synthesis of Potential Odorants Derived From Manool | Australian Journal of Chemistry | 1994 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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