Chemical Properties of 24-Methyl-31-nor-9(11)-lanostenol acetate

24-Methyl-31-nor-9(11)-lanostenol acetate

InChI
InChI=1S/C32H54O2/c1-10-21(2)11-12-22(3)24-15-19-32(9)26-13-14-27-29(5,6)28(34-23(4)33)17-18-30(27,7)25(26)16-20-31(24,32)8/h16,21-22,24,26-28H,10-15,17-20H2,1-9H3/t21?,22-,24?,26?,27?,28-,30+,31+,32-/m0/s1
InChI Key
WLHVUZHSICZLPG-FOIYUBGNSA-N
Formula
C32H54O2
SMILES
CCC(C)CC[C@H](C)C1CC[C@@]2(C)C3CCC4C(C)(C)[C@@H](OC(C)=O)CC[C@]4(C)C3=CC[C@]12C
Molecular Weight1
470.78
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
Δfus 37.92 kJ/mol Joback Calculated Property
logPoct/wat 8.986 Crippen Calculated Property
McVol 421.440 ml/mol McGowan Calculated Property
Inp [3369.00; 3369.00]   Show Hide
Inp 3369.00 NIST
Inp 3369.00 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 [1656.55; 2002.94] J/mol×K [1023.83; 1258.99] Show Hide
Cp,gas 1656.55 J/mol×K 1023.83 Joback Calculated Property
Cp,gas 1704.26 J/mol×K 1063.02 Joback Calculated Property
Cp,gas 1755.19 J/mol×K 1102.22 Joback Calculated Property
Cp,gas 1809.94 J/mol×K 1141.41 Joback Calculated Property
Cp,gas 1869.09 J/mol×K 1180.60 Joback Calculated Property
Cp,gas 1933.23 J/mol×K 1219.79 Joback Calculated Property
Cp,gas 2002.94 J/mol×K 1258.99 Joback Calculated Property

Similar Compounds

31-Nor-9(11)-lanostenol acetate. 24-Dihydroparkeol acetate. Trematol (21-epi-9[11]-fernenol) acetate. Epifernenol (9[11]-fernen-3A-ol) acetate. Fernenol (9[11]-fernenol) acetate. Lanost-9(11)-en-3-ol, acetate, (3«beta»,8«alpha»,13«alpha»,14«beta»,17«alpha»)-. 24,25-Dimethyl-9(11)-lanostenol acetate. 24,24-Dimethyl-9(11)-lanostenol acetate. 24-Methyl-24-dihydroparkeol acetate. 24-Methyl-31-nor-7-lanostenol acetate. 31-Nor-7-lanosterol acetate. 7-Tirucallenol acetate. Lanost-7-en-3-ol, acetate, (3«beta»,9«beta»,13«alpha»,14«beta»,17«alpha»)-. Lanost-7-en-3-ol, acetate, (3«beta»)-. 24-Methylene-24-dihydroparkeol acetate.

Find more compounds similar to 24-Methyl-31-nor-9(11)-lanostenol 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.