3D model (JSmol)
|Molar mass||204.357 g·mol−1|
|Boiling point||124 °C (255 °F; 397 K) (15 mmHg)|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
Copaene, or more precisely, α-copaene, is the common (or trivial) chemical name of an oily liquid hydrocarbon that is found in a number of essential oil-producing plants. The name is derived from that of the resin-producing tropical copaiba tree, Copaifera langsdorfii, from which the compound was first isolated in 1914. Its structure, including the chirality, was determined in 1963. The double-bond isomer with an exocyclic-methylene group, β-copaene, was first reported in 1967.
Chemically, the copaenes are tricyclic sesquiterpenes. The molecules are chiral, and the α-copaene enantiomer most commonly found in higher plants exhibits a negative optical rotation of about −6°. The rare (+)-α-copaene is also found in small amounts in some plants. It is of economic significance because it is strongly attracting to an agricultural pest, the Mediterranean fruit fly Ceratitis capitata.
- V.H. Kapadia; Nagasampagi, B.A.; Naik, V.G.; Dev, Sukh; et al. (1963). "Structure of mustakone and copaene". Tetrahedron Letters. 4 (28): 1933. doi:10.1016/S0040-4039(01)90945-1.
- L. Westfelt; Westfelt, Lars; Sky, K.; Nilsson, Åke; Theorell, H.; Blinc, R.; Paušak, S.; Ehrenberg, L.; Dumanović, J. (1967). "Beta-Copaene and beta-Ylangene, Minor Sesquiterpenes of the Wood of Pinus silvestris L. And of Swedish Sulphate Turpentine". Acta Chemica Scandinavica. 21: 152. doi:10.3891/acta.chem.scand.21-0152.
- R. Nishida; Shelly, Todd E.; Whittier, Timothy S.; Kaneshiro, Kenneth Y.; et al. (2000). Journal of Chemical Ecology. 26: 87. doi:10.1023/A:1005489411397. S2CID 44000579. Missing or empty