Abietane
From Wikipedia, the free encyclopedia
Abietane | |
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Other names 13α-Isopropylpodocarpane | |
Identifiers | |
CAS number | 19407-12-6 |
PubChem | 6857485 |
ChemSpider | 5256821 |
ChEBI | CHEBI:35673 |
Jmol-3D images | {{#if:[H][C@]12[C@@](C[C@@H](C(C)C)CC2)([H])CC[C@@]3([H])C(C)(C)CCC[C@@]31C|Image 1 |
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Properties | |
Molecular formula | C20H36 |
Molar mass | 276.50 g mol−1 |
Density | 0.876 g/ml |
Melting point | 338 °C; 640 °F; 611 K |
(verify) (what is: / ?) Except where noted otherwise, 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.
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