- Cubebol
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Cubebol 
(3S,3aR,3bR,4S,7R,7aR)-Octahydro-3,7-dimethyl-4-(1-methylethyl)-1H-cyclopenta[1,3]cyclopropa[1,2]benzen-3-olIdentifiers CAS number 23445-02-5 PubChem 11276107 ChemSpider 9451107 
Jmol-3D images Image 1
Image 2- [H][C@]12[C@H]([C@H](C)C)CC[C@@H](C)[C@]31[C@@]([H])2[C@@](C)(O)CC3
O[C@]3(CC[C@@]12[C@@H](CC[C@H]([C@@H]1[C@H]23)C(C)C)C)C
- InChI=1S/C15H26O/c1-9(2)11-6-5-10(3)15-8-7-14(4,16)13(15)12(11)15/h9-13,16H,5-8H2,1-4H3/t10-,11+,12-,13+,14+,15-/m1/s1
Key: KONGRWVLXLWGDV-BYGOPZEFSA-N
InChI=1/C15H26O/c1-9(2)11-6-5-10(3)15-8-7-14(4,16)13(15)12(11)15/h9-13,16H,5-8H2,1-4H3/t10-,11+,12-,13+,14+,15-/m1/s1
Key: KONGRWVLXLWGDV-BYGOPZEFBC
Properties Molecular formula C15H26O Molar mass 222.37 g/mol Melting point 61-62 °C
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Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)Infobox references Cubebol is a natural sesquiterpene alcohol first identified in cubeb oil. It was patented as a cooling agent in 2001 by Firmenich, an international flavor company. The taste of cubebol is cooling and refreshing.[1] The patent describes application of cubebol as a refreshing agent in various products, ranging from chewing gum to sorbets, drinks, toothpaste, and gelatin-based confectioneries.[2]
References
- ^ Leffingwell, John C., Ph.D (2001). "Cool without Menthol & Cooler than Menthol and Cooling Compounds as Insect Repellents". Leffingwell & Associates. http://www.leffingwell.com/cooler_than_menthol.htm. Retrieved 2006-09-15.
- ^ U.S. Patent 6,214,788
Categories:- Cooling flavors
- Alcohols
- Sesquiterpenes
- [H][C@]12[C@H]([C@H](C)C)CC[C@@H](C)[C@]31[C@@]([H])2[C@@](C)(O)CC3
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