Chemical Properties of 31-Nor-9(11)-lanostenol acetate

31-Nor-9(11)-lanostenol acetate

InChI
InChI=1S/C31H52O2/c1-9-10-11-12-21(2)23-15-19-31(8)25-13-14-26-28(4,5)27(33-22(3)32)17-18-29(26,6)24(25)16-20-30(23,31)7/h16,21,23,25-27H,9-15,17-20H2,1-8H3/t21-,23?,25?,26?,27-,29+,30+,31-/m1/s1
InChI Key
IMUXJQPSVOGFLZ-MWDIYCQFSA-N
Formula
C31H52O2
SMILES
CCCCCC(C)C1CCC2(C)C3CCC4C(C)(CCC(OC(C)=O)C4(C)C)C3=CCC12C
Molecular Weight1
456.74
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° 38.86 kJ/mol Joback Calculated Property
logPoct/wat 8.740 Crippen Calculated Property
McVol 407.350 ml/mol McGowan Calculated Property
Inp [3275.00; 3275.00]   Show Hide
Inp 3275.00 NIST
Inp 3275.00 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 [1578.32; 1901.66] J/mol×K [1001.39; 1233.70] Show Hide
Cp,gas 1578.32 J/mol×K 1001.39 Joback Calculated Property
Cp,gas 1623.12 J/mol×K 1040.11 Joback Calculated Property
Cp,gas 1670.82 J/mol×K 1078.83 Joback Calculated Property
Cp,gas 1721.96 J/mol×K 1117.55 Joback Calculated Property
Cp,gas 1777.10 J/mol×K 1156.27 Joback Calculated Property
Cp,gas 1836.82 J/mol×K 1194.98 Joback Calculated Property
Cp,gas 1901.66 J/mol×K 1233.70 Joback Calculated Property

Similar Compounds

24-Methyl-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 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.