Chemical Properties of exo-Tricyclo[6,2,1,0(2,6)]decan-8-«beta»-ol, acetate

exo-Tricyclo[6,2,1,0(2,6)]decan-8-«beta»-ol, acetate

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InChI
InChI=1S/C12H18O2/c1-7(13)14-12-6-8-5-11(12)10-4-2-3-9(8)10/h8-12H,2-6H2,1H3/t8?,9-,10-,11?,12+/m0/s1
InChI Key
YKFHIJHJBUDXFP-MUVKAJBYSA-N
Formula
C12H18O2
SMILES
CC(=O)OC1CC2CC1C1CCCC21
Molecular Weight1
194.27
Sources

Physical Properties

Property Value Unit Source
Δf -29.03 kJ/mol Joback Calculated Property
Δfgas -364.25 kJ/mol Joback Calculated Property
Δfus 24.07 kJ/mol Joback Calculated Property
Δvap 50.75 kJ/mol Joback Calculated Property
logPoct/wat 2.374 Crippen Calculated Property
Pc 2563.69 kPa Joback Calculated Property
Tboil 565.40 K Joback Calculated Property
Tc 779.60 K Joback Calculated Property
Tfus 338.98 K Joback Calculated Property
Vc 0.593 m3/kg-mol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas 426.54 J/mol×K 565.4 Joback Calculated Property
η 0.0021114 Pa×s 565.4 Joback Calculated Property

Molecular Descriptors

Joback and Reid Groups
-O- (nonring) 1
-CH3 1
>CH- (ring) 5
-CH2- (ring) 5
>C=O (nonring) 1

Similar Compounds

exo-Tricyclo[6,2,1,0(2,6)]decan-8-«alpha»-ol, acetate. endo-Tricyclo[6,2,1,0(2,6)]decan-8-«alpha»-ol, acetate. endo-Tricyclo[6,2,1,0(2,6)]decan-8-«beta»-ol, acetate. endo-2-norborneol acetate. 2-Norbornyl acetate. Cyclohexanol, 5-methyl-2-(1-methylethyl)-, acetate. Acetic acid, p-menth-3-yl ester. Cyclohexanol, 5-methyl-2-(1-methylethyl)-, acetate, (1«alpha»,2«alpha»,5«beta»)-. Cyclohexanol, 5-methyl-2-(1-methylethyl)-, acetate, (1«alpha»,2«beta»,5«beta»)-. Menthyl acetate. Neoisomenthyl acetate. isobornyl propanoate. 5«alpha»-Cholestan-3«alpha»-ol, 4«alpha»-methyl-, acetate. Neocarvomenthyl acetate. Neoisocarvomenthyl acetate.

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