Misplaced Pages

Cembrene A

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
(Redirected from Neo-cembrene)
Cembrene A
Cembrene A
Names
Preferred IUPAC name (1E,5E,9E,12R)-1,5,9-Trimethyl-12-(prop-1-en-2-yl)cyclotetradeca-1,5,9-triene
Other names (R,1E,5E,9E)-1,5,9-Trimethyl-12-(prop-1-en-2-yl)cyclotetradeca-1,5,9-triene
Neocembrene-A
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
PubChem CID
UNII
InChI
  • InChI=1/C20H32/c1-16(2)20-14-12-18(4)10-6-8-17(3)9-7-11-19(5)13-15-20/h8,11-12,20H,1,6-7,9-10,13-15H2,2-5H3/b17-8+,18-12+,19-11+/t20-/m0/s1Key: VWSPQDDPRITBAM-KPGNMOGWBK
SMILES
  • C1(=C\CC/C(=C/C(C(=C)\C)CCC(=C\CC1)\C)C)\C
Properties
Chemical formula C20H32
Molar mass 272.47 g/mol
Boiling point 150 to 152 °C (302 to 306 °F; 423 to 425 K) at 0.8 mmHg
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

Cembrene A, or sometimes neocembrene, is a natural monocyclic diterpene isolated from corals of the genus Nephthea. It is a colorless oil with a faint wax-like odor.

Cembrene A itself has little importance as a chemical entity, being a trail pheromone for termites; however, the chemical structure of cembrene is central to a very wide variety of other natural products found both in plants and in animals. Pinus leucodermis tree bark and wood essential oils contain a high percentage of cembrene.

Cembrenes are biosynthesized by macrocyclization of geranylgeranyl pyrophosphate.

References

  1. Vanderah, David J.; Rutledge, Neal; Schmitz, Francis J.; Ciereszko, Leon S (1978). "Marine natural products: cembrene-A and cembrene-C from a soft coral, Nephthea species". Journal of Organic Chemistry. 43 (8): 1614–1616. doi:10.1021/jo00402a040.
  2. Birch, A. J.; Brown, W. V.; Corrie, J. E. T.; Moore, B. P (1972). "Neocembrene-A, a termite trail pheromone". Journal of the Chemical Society, Perkin Transactions 1. 21: 2653–2658. doi:10.1039/p19720002653.
  3. ^ Terpenes: Flavors, Fragrances, Pharmaca, Pheromones, Eberhard Breitmaier, page 7. ISBN 978-3-527-31786-8
  4. Graikou, K.; Gortzi, O.; Mantanis, G.; Chinou, I. (2012). "Chemical composition and biological activity of the essential oil from the wood of Pinus heldreichii Christ. var. leucodermis". European Journal of Wood and Wood Products. 70 (5): 615–620. doi:10.1007/s00107-012-0596-9. ISSN 0018-3768.
Categories: