Chemical Properties of Isoarborinol (9[11]-arborinenol) acetate

Isoarborinol (9[11]-arborinenol) acetate

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InChI Key
Molecular Weight1
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Physical Properties

Property Value Unit Source
Δf 249.41 kJ/mol Joback Calculated Property
Δfgas -485.12 kJ/mol Joback Calculated Property
Δfus 31.61 kJ/mol Joback Calculated Property
Δvap 89.64 kJ/mol Joback Calculated Property
log10WS -9.20 Crippen Calculated Property
logPoct/wat 8.516 Crippen Calculated Property
McVol 406.280 ml/mol McGowan Calculated Property
Pc 909.43 kPa Joback Calculated Property
Inp 3468.00 NIST
Tboil 1045.72 K Joback Calculated Property
Tc 1295.30 K Joback Calculated Property
Tfus 687.00 K Joback Calculated Property
Vc 1.542 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [1654.61; 2121.55] J/mol×K [1045.72; 1295.30] Show Hide
Cp,gas 1654.61 J/mol×K 1045.72 Joback Calculated Property
Cp,gas 1715.01 J/mol×K 1087.32 Joback Calculated Property
Cp,gas 1781.25 J/mol×K 1128.91 Joback Calculated Property
Cp,gas 1854.17 J/mol×K 1170.51 Joback Calculated Property
Cp,gas 1934.63 J/mol×K 1212.11 Joback Calculated Property
Cp,gas 2023.47 J/mol×K 1253.70 Joback Calculated Property
Cp,gas 2121.55 J/mol×K 1295.30 Joback Calculated Property

Similar Compounds

24-Methylene-24-dihydroparkeol acetate. 24-Methylene-31-nor-9(11)-lanostenol acetate. Lanosta-9(11),24-dien-3-ol, acetate, (3«beta»)-. 24,24-Dimethyl-9(11),25-lanostadienol acetate. 24-Methyl-31-nor-9(11)-lanostenol acetate. 31-Nor-9(11)-lanostenol acetate. Trematol (21-epi-9[11]-fernenol) acetate. 24-Dihydroparkeol acetate. Fernenol (9[11]-fernenol) acetate. 24,25-Dimethyl-9(11)-lanostenol acetate. 24-Methyl-24-dihydroparkeol acetate. Epifernenol (9[11]-fernen-3A-ol) acetate. 24,24-Dimethyl-9(11)-lanostenol acetate. Lanost-9(11)-en-3-ol, acetate, (3«beta»,8«alpha»,13«alpha»,14«beta»,17«alpha»)-. Butyrospermol acetate.

Find more compounds similar to Isoarborinol (9[11]-arborinenol) acetate.


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