Chemical Properties of 24-Methylene-24-dihydroparkeol acetate

24-Methylene-24-dihydroparkeol acetate

InChI
InChI=1S/C33H54O2/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,3,11-15,17-20H2,1-2,4-10H3/t23?,25-,27?,28-,29?,31?,32?,33-/m0/s1
InChI Key
VXHAOJSMBYBPDB-JUXMHOGSSA-N
Formula
C33H54O2
SMILES
C=C(CCC(C)[C@@H]1CC[C@@]2(C)C3CC[C@@H]4C(C)(CCC(OC(C)=O)C4(C)C)C3=CCC12C)C(C)C
Molecular Weight1
482.79
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° 37.92 kJ/mol Joback Calculated Property
logPoct/wat 9.152 Crippen Calculated Property
McVol 431.230 ml/mol McGowan Calculated Property
Inp [3428.00; 3428.00]   Show Hide
Inp 3428.00 NIST
Inp 3428.00 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.

Correlations

Property Value Unit Temperature (K) Source
Cp,gas [582.78; 1651.69] J/mol×K [273.00; 1000.00] Joback Predicted correlation Show Hide
EquationY = A + B·T + C·T² + D·T³ + E·T⁴
Y is Cp,gas in J/mol×K, T in K
Coefficient A-3.88448e+02
Coefficient B4.57758e+00
Coefficient C-4.18624e-03
Coefficient D1.64880e-06
Coefficient E0.00000e+00
Temperature range, min.273.00
Temperature range, max.1000.00
Cp,gas 582.78 J/mol×K 273.00 Calculated Property
Cp,gas 780.06 J/mol×K 353.78 Calculated Property
Cp,gas 945.54 J/mol×K 434.56 Calculated Property
Cp,gas 1084.45 J/mol×K 515.33 Calculated Property
Cp,gas 1201.99 J/mol×K 596.11 Calculated Property
Cp,gas 1303.37 J/mol×K 676.89 Calculated Property
Cp,gas 1393.82 J/mol×K 757.67 Calculated Property
Cp,gas 1478.55 J/mol×K 838.44 Calculated Property
Cp,gas 1562.77 J/mol×K 919.22 Calculated Property
Cp,gas 1651.69 J/mol×K 1000.00 Calculated Property

Similar Compounds

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

Find more compounds similar to 24-Methylene-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.