6-BETA-ACETOXY-11,12-EPOXY-4-BETA-HYDROXYEUDESMAN-1-ONE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 8jJdnxZXdhy |
|---|---|
| InChI | InChI=1S/C17H26O5/c1-10(18)22-13-11(17(4)9-21-17)5-7-15(2)12(19)6-8-16(3,20)14(13)15/h11,13-14,20H,5-9H2,1-4H3/t11-,13-,14?,15+,16+,17?/m1/s1 |
| InChIKey | AZCDEYVPRTYQFA-GGYHRCHZSA-N |
| Mol Weight | 310.39 g/mol |
| Molecular Formula | C17H26O5 |
| Exact Mass | 310.178024 g/mol |
| Enantiomer InChIKey | AZCDEYVPRTYQFA-KIOSQEFBSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
4-EPI-ARGLANIN
(3S,3AS,5AS,9R*,9AR,9BS)-9-METHOXY-3,5A,9-TRIMETHYL-OCTAHYDRO-NAPHTHO-[1,2-B]-FURAN-2,6-DIONE
TAUREMISIN,ACETYL,TETRAHYDRO
DICTAMNOSIDE-J
DICTAMNOSIDE-I
5-A-H,11-B-H-EIDESMAN-12,6-A-OLIDE,2-B-ACETOXY-4-A-METHOXYCARBONYL
4-EPI-VULGARIN
NGPDZEACIWDCKX-FWPUEQERSA-N
BARRELIN
10-Isopropyl-8-acetoxy-5-benzoyloxy-3,7-dimethylhexahydro-1H-azeluene-10-ol
| Title | Journal or Book | Year |
|---|---|---|
| Chemical-Microbiological Synthesis of Cryptomeridiol Derivatives by Gliocladium roseum: Semisynthesis of 11-Hydroxyeudesmanolides | Journal of Natural Products | 2002 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
The KnowItAll NMR Spectral Library offers a comprehensive collection of NMR reference spectra, including NMR, CNMR, and XNMR, and covers a wide range of compounds including organics, polymers, monomers, metabolites, and more. Learn more.