ENT-3-BETA-ACETOXY-12-BETA-HYDROXY-13-EPI-MANOYL-OXIDE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | AS9MZrzweFX |
|---|---|
| InChI | InChI=1S/C22H36O4/c1-8-21(6)17(24)13-16-20(5)11-10-18(25-14(2)23)19(3,4)15(20)9-12-22(16,7)26-21/h8,15-18,24H,1,9-13H2,2-7H3/t15-,16+,17+,18-,20-,21+,22+/m1/s1 |
| InChIKey | RQAKPAGNCKWNAV-QKYFFWMQSA-N |
| Mol Weight | 364.5 g/mol |
| Molecular Formula | C22H36O4 |
| Exact Mass | 364.26136 g/mol |
| Enantiomer InChIKey | RQAKPAGNCKWNAV-XCUGWHMJSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
ENT-3-BETA,12-BETA,18-TRIHYDROXY-13-EPI-MANOYL-OXIDE
ent-12.alpha.Hydroxy-3-oxo-13-epi-manoyl oxide
(14S)-ent-8,13.beta.-Epoxylabdane-3.beta.,12.beta.,14-triol
(14R)-ent-8,13.beta.-Epoxylabdane-3.beta.,12.beta.,14-triol
(14R)-ent-8,13.beta.-Epoxylabdane-3.beta.,12.alpha.,14-triol
EXCOECARIN-S;13-EPI-12-HYDROXY-2,3-SECOLABDA-14-ENE
1H-Naphtho[2,1-b]pyran, 2(5H)-furanone deriv.
ENT-13-EPI-8,13-EPOXY-3-BETA,14S,15-TRIACETOXYLABDANE
| Title | Journal or Book | Year |
|---|---|---|
| Chemical-microbiological synthesis of ent-13-epi-manoyl oxides with biological activities | Phytochemistry | 1994 |
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.