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

Isoarborinol (9[11]-arborinenol) acetate

InChI
InChI=1S/C32H50O2/c1-20(2)22-10-13-26-30(22,7)18-19-31(8)24-11-12-25-28(4,5)27(34-21(3)33)15-16-29(25,6)23(24)14-17-32(26,31)9/h14,22,24-27H,1,10-13,15-19H2,2-9H3/t22-,24?,25-,26?,27-,29+,30?,31+,32?/m0/s1
InChI Key
HGJARKCTVXMQKJ-OHLBPESASA-N
Formula
C32H50O2
SMILES
C=C(C)[C@@H]1CCC2C1(C)CC[C@]1(C)C3CC[C@H]4C(C)(C)[C@@H](OC(C)=O)CC[C@]4(C)C3=CCC21C
Molecular Weight1
466.75
Cheméo is a service of Céondo GmbH, since 2007, we provide simulation, modelling and software development services for the industry. Do not hesitate to contact us for your projects.

Physical Properties

Property Value Unit Source
ΔfusH° 33.19 kJ/mol Joback Calculated Property
logPoct/wat 8.516 Crippen Calculated Property
McVol 406.280 ml/mol McGowan Calculated Property
Inp 3468.00 NIST

Cheméo can also estimate Normal Boiling Point Temperature, Normal melting (fusion) point, Critical Temperature, Critical Pressure, Critical Volume, Enthalpy of formation at standard conditions, Enthalpy of vaporization at standard conditions, Standard Gibbs free energy of formation, Acentric Factor, Ionization energy, Log10 of Water solubility in mol/l for this compound, but they fall outside the models' validated range, so they are not shown here. Open the prediction tool to compute them on demand.

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [1630.44; 2069.04] J/mol×K [1027.85; 1275.30] Show Hide
Cp,gas 1630.44 J/mol×K 1027.85 Joback Calculated Property
Cp,gas 1687.46 J/mol×K 1069.09 Joback Calculated Property
Cp,gas 1749.81 J/mol×K 1110.33 Joback Calculated Property
Cp,gas 1818.30 J/mol×K 1151.57 Joback Calculated Property
Cp,gas 1893.79 J/mol×K 1192.81 Joback Calculated Property
Cp,gas 1977.09 J/mol×K 1234.06 Joback Calculated Property
Cp,gas 2069.04 J/mol×K 1275.30 Joback Calculated Property

Similar Compounds

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

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

Sources

Note: Cheméo is only indexing the data, follow the source links to retrieve the latest data. The source is also providing more information like the publication year, authors and more. Take the time to validate and double check the source of the data.
These property values are available through the Cheméo API. A free account gives you an access key.