| Identification | Back Directory | [Name]
3,5,5-TRIMETHYL-2-CYCLOHEXEN-1-OL | [CAS]
470-99-5 | [Synonyms]
AKOS 50
ISOPHOROL
3,5,5-triMethylcyclohex-2-enol
1,5,5-Trimethylcyclohexene-3-ol
3,5,5-trimethyl-2-cyclohexen-1-o
3,5,5-trimethylcyclohex-2-en-1-ol
3,5,5-TRIMETHYL-2-CYCLOHEXEN-1-OL
3,5,5-Trimethyl-2-cyclohexen-1-ol,95% | [EINECS(EC#)]
207-433-6 | [Molecular Formula]
C9H16O | [MDL Number]
MFCD00001554 | [MOL File]
470-99-5.mol | [Molecular Weight]
140.22 |
| Hazard Information | Back Directory | [Chemical Properties]
clear colorless liquid | [Uses]
This alcohol has found a little use in perfume compositions, mainly in Honey-bases as a modifier and powerful ingredient. It blends excellently with Phenylacetic acid and its esters, with Mimosa, Labdanum and the conventional Acetophenone-derivatives, and it is, incidentally, very interesting in YlangYlang. | [Synthesis Reference(s)]
Journal of the American Chemical Society, 100, p. 2226, 1978 DOI: 10.1021/ja00475a040
The Journal of Organic Chemistry, 47, p. 3311, 1982 DOI: 10.1021/jo00138a021 | [General Description]
3,5,5-Trimethyl-2-cyclohexen-1-ol undergoes oxidation in the presence of palladium on activated charcoal under an ethylene atmosphere to yield the corresponding carbonyl compound. | [Synthesis]
3,5,5-Trimethyl-2-cyclohexen-1-ol is prepared (several methods) e. g. from isoPhorone by controlled hydrogenation. It has also been prepared from 3,3-Dimethyl cyclohexanol. |
| Spectrum Detail | Back Directory | [Spectrum Detail]
3,5,5-TRIMETHYL-2-CYCLOHEXEN-1-OL(470-99-5)MS
3,5,5-TRIMETHYL-2-CYCLOHEXEN-1-OL(470-99-5)1HNMR
3,5,5-TRIMETHYL-2-CYCLOHEXEN-1-OL(470-99-5)13CNMR
3,5,5-TRIMETHYL-2-CYCLOHEXEN-1-OL(470-99-5)IR1
3,5,5-TRIMETHYL-2-CYCLOHEXEN-1-OL(470-99-5)Raman
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Energy Chemical
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Sigma-Aldrich
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