| Identification | Back Directory | [Name]
α-fenchylalcohol,endo-1,3,3-trimethyl-norbornan-2-ol,1,3,3-trimethyl-bicyclo[2.2.1]heptan-2-ol | [CAS]
14575-74-7 | [Synonyms]
(±)-α-Fenchol
Bicyclo[2.2.1]heptan-2-ol, 1,3,3-trimethyl-, (1R,2R,4S)-rel-
α-fenchylalcohol,endo-1,3,3-trimethyl-norbornan-2-ol,1,3,3-trimethyl-bicyclo[2.2.1]heptan-2-ol
α-fenchylalcohol,α-fenchylalcoholα-1,3,3-trimethyl-norbornan-2-ol,α-1,3,3-trimethylbicyclo[2.2.1]heptan-2-ol | [Molecular Formula]
C10H18O | [MOL File]
14575-74-7.mol | [Molecular Weight]
154.25 |
| Chemical Properties | Back Directory | [storage temp. ]
Refrigerator | [solubility ]
Chloroform (Sparingly), DMSO (Slightly), Ethanol (Sparingly), Methanol (Slightly | [form ]
Solid | [color ]
Colourless to Off-White Semi-Solid | [Odor]
camphor | [LogP]
2.707 (est) |
| Hazard Information | Back Directory | [Uses]
(±)-α-Fenchol is found in essential oils from many plants. It has been studied for, insecticidal activity of essential oil from Helichrysum faradifani; antioxidant and antibacterial activity of essential oils from rhizome, leaf and stem of Etlingera sayapensis against growth of Bacillus subtilis, Escherichia coli and Candida albicans. | [Definition]
ChEBI: (-)-endo-fenchol is a fenchane monoterpenoid that is bicyclo[2.2.1]heptane substituted by methyl groups at positions 1, 3 and 3 and a hydroxy group at position 2 (the 1S,2S,4R stereoisomer). It has a role as a plant metabolite and a volatile oil component. It is a fenchane monoterpenoid and a carbobicyclic compound. |
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