Retronecine
Names | |
---|---|
IUPAC name
(1R,7aR)-7-(Hydroxymethyl)-2,3,5,7a-tetrahydro-1H-pyrrolizin-1-ol | |
Other names
(+)-Retronecine; Retronecin; Senecifolinene | |
Identifiers | |
480-85-3 | |
3D model (Jmol) | Interactive image |
ChemSpider | 9783 |
PubChem | 10198 |
| |
| |
Properties | |
C8H13NO2 | |
Molar mass | 155.20 g·mol−1 |
Melting point | 119 to 120 °C (246 to 248 °F; 392 to 393 K)[1] |
Hazards | |
Lethal dose or concentration (LD, LC): | |
LD50 (median dose) |
634 mg/kg (IV, mouse)[1] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Retronecine is a pyrrolizidine alkaloid found in a variety of plants in the genera Senecio and Crotalaria, and the family Boraginaceae. It is the most common central core for other pyrrolizidine alkaloids.[1]
References
- 1 2 3 Retronecine, Merck Index, 12th Edition, 8334
This article is issued from Wikipedia - version of the 6/23/2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.