ChemicalBook--->CAS DataBase List--->70788-30-6

70788-30-6

70788-30-6 Structure

70788-30-6 Structure
IdentificationBack Directory
[Name]

1-(2,2,6-Trimethylcyclohexyl)- hexan-3-ol
[CAS]

70788-30-6
[Synonyms]

Timberol
Temubeol
Finotimber
Termumetol
NORLIMBANOL
TIMBEROL TOUCH
timber propanol
1-(2,2,6-trimethylcyclohexyl)hexan-3-ol
1-(2,2,6-TRIMETHYLCYCLOHEXYL)-3-HEXANOL
6-(2,2,6-Trimethylcyclohexyl)-4-hexanol
1-(2,2,6-Trimethylcyclohexyl)hexane-3-ol
2,2,6-trimethyl-α-propylcyclohexanepropanol
α-Propyl-2,2,6-trimethyl-cyclohexanepropanol
Cyclohexanepropanol,2,2,6-trimethyl-a-propyl-
2,2,6-Trimethyl-alpha-propylcyclohexanpropanol
Cyclohexanepropanol, 2,2,6-trimethyl-α-propyl-
2,2,6-Trimethyl-α-propylcyclohexane-1-propanol
2,2,6-trimethyl-alpha-propyl-cyclohexanepropano
2,2,6-trimethyl-.alpha.-propyl-Cyclohexanepropanol
Cyclohexanepropanol, 2,2,6-trimethyl-.alpha.-propyl-
[EINECS(EC#)]

274-892-7
[Molecular Formula]

C15H30O
[MDL Number]

MFCD01451532
[MOL File]

70788-30-6.mol
[Molecular Weight]

226.4
Chemical PropertiesBack Directory
[Boiling point ]

280℃
[density ]

0.850
[Fp ]

124℃
[pka]

15.24±0.20(Predicted)
[Odor]

at 100.00 %. dry sawdust woody powdery amber sandalwood
[Odor Type]

woody
[LogP]

5.635 (est)
[EPA Substance Registry System]

Cyclohexanepropanol, 2,2,6-trimethyl-.alpha.-propyl- (70788-30-6)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H317
[Precautionary statements ]

P261-P272-P280-P302+P352-P333+P313-P321-P363-P501
Hazard InformationBack Directory
[Chemical Properties]

1-(2,2,6-Trimethylcyclohexyl)- hexan-3-ol is a colorless liquid with a highly diffusive, powdery, woody odor. It is amixture of the cis- and trans-isomers. The trans-isomer has a more distinct animal and amber character.
The title compound is prepared by condensation of citral with 2- pentanone in the presence of bases to give 8,12-dimethyltrideca-5,7,11-trien-4- one, which is cyclized and hydrogenated.
A high-trans mixture can be prepared starting from ??-cyclocitral, which is hydrogenated to 2,2,6-trimethylcyclohexane carboxaldehyde. Condensation with 2-pentanone in the presence of sodium ethoxide yields the corresponding 3-hexenone. Hydrogenation with nickel–copper chromite as a catalyst gives a mixture with up to 95% of the trans-isomer.
It is used in perfume compositions for soaps, detergents, and household products.
[Trade name]

Norlimbanol® (Firmenich), Timberol® (Symrise)
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