8.alpha.,13-epoxylabdano-15,12.alpha.-lactone
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 7Av2Tri5jjG |
|---|---|
| InChI | InChI=1S/C20H32O3/c1-17(2)8-6-9-18(3)13(17)7-10-19(4)14(18)11-15-20(5,23-19)12-16(21)22-15/h13-15H,6-12H2,1-5H3/t13-,14+,15-,18-,19+,20-/m0/s1 |
| InChIKey | UZEQEUJYTWPLTK-XGVHXEIDSA-N |
| Mol Weight | 320.5 g/mol |
| Molecular Formula | C20H32O3 |
| Exact Mass | 320.235145 g/mol |
| Enantiomer InChIKey | UZEQEUJYTWPLTK-BEYYYLICSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | Unknown |
15-ACETOXY-13-EPI-MANOYLOXIDE-14-O-ALPHA-L-ARABINOPYRANOSIDE;TARAPACOL-15-ACETATE-14-O-ALPHA-L-ARABINOPYRANOSIDE
Silphanexopol - 15,16-diacetate
SILPHANEPOXOL-DIACETATE
TARAPACANONE;14-HYDROXY-15-ACETOXY-11-KETO-13-EPI-MANOYLOXIDE
ENT-3-BETA,12-BETA,18-TRIHYDROXY-13-EPI-MANOYL-OXIDE
Cyclo-schkuhriadiol 16-O-acetate
ENT-13-EPI-8,13-EPOXY-3-BETA,14S,15-TRIACETOXYLABDANE
Chlorosilphanol A - 15,16-Diacetate
3-Oxo-3'-oxa-14S,15-epoxy-ent-A-homo-13-epi-monoyl oxide
(14R)-8,13;14,15-DIEPOXYLABDANE-7-BETA-OL
| Title | Journal or Book | Year |
|---|---|---|
| Conversion of Manoyl Oxide Into 12-β-Hydroxymanoyl Oxide | Australian Journal of Chemistry | 1991 |
This compound is available in the following databases:
Wiley Registry of Mass Spectral Data 2023
Author: Wiley
The foundation library for any analytical laboratory running mass spectrometry, the Wiley Registry provides the broadest coverage available in any mass spectral library Learn more.