DIOSGENINACETAT=(25R)-3-BETA-ACETOXY-5-SPIROSTEN
Compound with spectra: 2 NMR
| SpectraBase Compound ID | K1Nj8emqPjU |
|---|---|
| InChI | InChI=1S/C29H44O4/c1-17-8-13-29(31-16-17)18(2)26-25(33-29)15-24-22-7-6-20-14-21(32-19(3)30)9-11-27(20,4)23(22)10-12-28(24,26)5/h6,17-18,21-26H,7-16H2,1-5H3/t17-,18-,21-,22+,23-,24-,25-,26-,27-,28-,29+/m0/s1 |
| InChIKey | CZCROZIJKBXZDP-RJTQZQFYSA-N |
| Mol Weight | 456.7 g/mol |
| Molecular Formula | C29H44O4 |
| Exact Mass | 456.32396 g/mol |
| Enantiomer InChIKey | CZCROZIJKBXZDP-CJXRVVNOSA-N |
| 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 |
- Diosgenin acetate
| Title | Journal or Book | Year |
|---|---|---|
| Carbon-13 NMR spectroscopy of steroidal sapogenins and steroidal saponins | Phytochemistry | 1985 |
| The Synthesis of (25R)-22αN-[15ξ,17α-2H2]-Spirosol-5-en-3β-ol ([15ξ,17α-2H2] Solasodine) and Assignment of the 13C N.M.R. Spectra of Solasodine and its Derivatives | Australian Journal of Chemistry | 1979 |
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