Digitoxigenin
Names | |
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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 | |
3D model (JSmol) |
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95448 | |
ChemSpider | |
ECHA InfoCard | 100.005.095 |
EC Number | 205-603-4 |
PubChem CID |
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RTECS number | FH4975000 |
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Properties | |
C23H34O4 | |
Molar mass | 374.51 |
Appearance | solid |
Melting point | 252 to 253 °C (486 to 487 °F; 525 to 526 K) |
Hazards | |
Main hazards | Toxic |
R-phrases (outdated) | Toxic if swallowed |
S-phrases (outdated) | In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
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
- ↑ http://www.sigmaaldrich.com/catalog/ProductDetail.do?N4=D9404%7CSIGMA&N5=SEARCH_CONCAT_PNO%7CBRAND_KEY&F=SPEC
- ↑ Ferland, J. M. (1974). "Synthetic Cardenolides and Related Products. III. Isocardenolides". Canadian Journal of Chemistry. 52 (9): 1652–1661. ISSN 0008-4042. doi:10.1139/v74-239.
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