(organic chemistry) C15H24 A colorless liquid that boils at 274.5°C, and is a terpene derived from cubeb oil, cade oil, juniper berry oil, and other essential oils.
| Sci-Tech Dictionary: cadinene |
(organic chemistry) C15H24 A colorless liquid that boils at 274.5°C, and is a terpene derived from cubeb oil, cade oil, juniper berry oil, and other essential oils.
| 5min Related Video: Cadinene |
| Wikipedia: Cadinene |
|
|
This article does not cite any references or sources. Please help improve this article by adding citations to reliable sources. Unsourced material may be challenged and removed. (September 2007) |
| (+)-α-Cadinene | |
|---|---|
| IUPAC name |
(1S,4aR,8aR)-4,7-dimethyl-1-(propan-2-yl)- 1,2,4a,5,6,8a-hexahydronaphthalene
|
| Properties | |
| Molecular formula | C15H24 |
| Molar mass | 204.35 g mol−1 |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
| Infobox references | |
| γ-Cadinene | |
|---|---|
| IUPAC name |
(1S,4aR,8aR)-7-methyl-4-methylidene-1- (propan-2-yl)-1,2,3,4,4a,5,6,8a-octahydronaphthalene
|
| Properties | |
| Molecular formula | C15H24 |
| Molar mass | 204.35 g mol−1 |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
| Infobox references | |
| δ-Cadinene | |
|---|---|
| IUPAC name |
(1S,8aR)-4,7-dimethyl-1-(propan-2-yl)- 1,2,3,5,6,8a-hexahydronaphthalene
|
| Properties | |
| Molecular formula | C15H24 |
| Molar mass | 204.35 g mol−1 |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
| Infobox references | |
Cadinene is the trivial chemical name of a number of isomeric hydrocarbons that occur in a wide variety of essential oil-producing plants. The name is derived from that of the Cade juniper (Juniperus oxycedrus L.), the wood of which yields an oil from which cadinene isomers were first isolated.
Chemically, the cadinenes are bicyclic sesquiterpenes. The term “cadinene” has sometimes been used in a broad sense to refer to any sesquiterpene with the so-called cadalane (4-isopropyl-1,6-dimethyldecahydronaphthalene) carbon skeleton. Because of the large number of known double-bond and stereochemical isomers, this class of compounds has been subdivided into four subclasses based on the relative stereochemistry at the isopropyl group and the two bridgehead carbon atoms. The name cadinene is now properly used only for the first subclass below, which includes the compounds originally isolated from cade oil. Only one enantiomer of each subclass is depicted, with the understanding that the other enantiomer bears the same subclass name.
This entry is from Wikipedia, the leading user-contributed encyclopedia. It may not have been reviewed by professional editors (see full disclaimer)
| oil of cubeb (materials) | |
| spruce oil (materials) | |
| (+)-delta-cadinene synthase |
| Why is cadinene in cigarettes? | |
| Can cadinene cause cancer? |
Copyrights:
![]() | Sci-Tech Dictionary. McGraw-Hill Dictionary of Scientific and Technical Terms. Copyright © 2003, 1994, 1989, 1984, 1978, 1976, 1974 by McGraw-Hill Companies, Inc. All rights reserved. Read more | |
![]() | Wikipedia. This article is licensed under the Creative Commons Attribution/Share-Alike License. It uses material from the Wikipedia article "Cadinene". Read more |