Chemical Properties of 24-Methyl-24-dihydroparkeol acetate

24-Methyl-24-dihydroparkeol acetate

InChI
InChI=1S/C33H56O2/c1-21(2)22(3)11-12-23(4)25-15-19-33(10)27-13-14-28-30(6,7)29(35-24(5)34)17-18-31(28,8)26(27)16-20-32(25,33)9/h16,21-23,25,27-29H,11-15,17-20H2,1-10H3/t22?,23?,25-,27?,28-,29?,31?,32?,33-/m0/s1
InChI Key
WDXFTQZWIULFAE-ZLXVBXEDSA-N
Formula
C33H56O2
SMILES
CC(=O)OC1CCC2(C)C3=CCC4(C)[C@H](C(C)CCC(C)C(C)C)CC[C@@]4(C)C3CC[C@H]2C1(C)C
Molecular Weight1
484.81
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 36.99 kJ/mol Joback Calculated Property
logPoct/wat 9.232 Crippen Calculated Property
McVol 435.530 ml/mol McGowan Calculated Property
Inp 3435.00 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 [1736.51; 2107.95] J/mol×K [1046.27; 1284.60] Show Hide
Cp,gas 1736.51 J/mol×K 1046.27 Joback Calculated Property
Cp,gas 1787.35 J/mol×K 1085.99 Joback Calculated Property
Cp,gas 1841.81 J/mol×K 1125.71 Joback Calculated Property
Cp,gas 1900.48 J/mol×K 1165.43 Joback Calculated Property
Cp,gas 1963.99 J/mol×K 1205.15 Joback Calculated Property
Cp,gas 2032.94 J/mol×K 1244.88 Joback Calculated Property
Cp,gas 2107.95 J/mol×K 1284.60 Joback Calculated Property

Similar Compounds

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

Find more compounds similar to 24-Methyl-24-dihydroparkeol 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.