Digitoxigenin
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| Names | |
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| IUPAC name
3β,14-Dihydroxy-5β-card-20(22)-enolide
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| Systematic IUPAC name
4-[(1R,3aS,3bR,5aR,7S,9aS,9bS,11aR)-5a,7-Dihydroxy-9a,11a-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-1-yl]furan-2(5H)-one | |
| Other names
3-β,14-dihydroxy-5-β,14-β-card-20(22)-enolide
5β-Card-20(22)-enolide, 3β,14-dihydroxy- Card-20(22)-enolide, 3,14-dihydroxy-, (3β,5β)- NSC 407806 Δ20:22-3,14,21-Trihydroxynorcholenic acid lactone cerberigenin echujetin evonogenin thevetigenin | |
| Identifiers | |
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3D model (JSmol)
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| 95448 | |
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PubChem CID
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| Properties | |
| C23H34O4 | |
| Molar mass | 374.51 |
| Appearance | solid[citation needed] |
| Melting point | 252 to 253 °C (486 to 487 °F; 525 to 526 K) |
| Hazards | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Template:Chembox Footer/trackingTemplate:Short description
Digitoxigenin, a cardenolide, is the aglycone of digitoxin.
Digitoxigenin can be used to prepare actodigin.[2]
In Lednicer's book on steroids, it is made from deoxycholic acid.
References
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- ^ http://www.sigmaaldrich.com/catalog/ProductDetail.do?N4=D9404%7CSIGMA&N5=SEARCH_CONCAT_PNO%7CBRAND_KEY&F=SPEC [dead link]
- ^ Page Module:Citation/CS1/styles.css has no content.Ferland, J. M. (1974). "Synthetic Cardenolides and Related Products. III. Isocardenolides". Canadian Journal of Chemistry. 52 (9): 1652–1661. doi:10.1139/v74-239. ISSN 0008-4042.
