Abietane
![]() | |
| Names | |
|---|---|
| Other names
13α-Isopropylpodocarpane | |
| Identifiers | |
| 19407-12-6 | |
| ChEBI | CHEBI:35673 |
| ChemSpider | 5256821 |
| Jmol interactive 3D | Image |
| PubChem | 6857485 |
| |
| |
| Properties | |
| C20H36 | |
| Molar mass | 276.51 g·mol−1 |
| Density | 0.876 g/ml |
| Melting point | 338 °C (640 °F; 611 K) |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| | |
| Infobox references | |
Abietane is a diterpene that forms the structural basis for a variety of natural chemical compounds such as abietic acid,[1] carnosic acid, and ferruginol which are collectively known as abietanes or abietane diterpenes.
See also
References
- ↑ San Feliciano, Arturo; Gordaliza, Marina; Salinero, Miguel A.; Miguel del Corral, Jose M (1993). "Abietane acids: sources, biological activities, and therapeutic uses". Planta Medica 59 (6): 485–490. doi:10.1055/s-2006-959744. PMID 8302943.
This article is issued from Wikipedia - version of the Tuesday, July 07, 2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.
