Chemical Properties of 11-Deoxycorticosterone, pivalate (CAS 808-48-0)

11-Deoxycorticosterone, pivalate

InChI
InChI=1S/C26H38O4/c1-24(2,3)23(29)30-15-22(28)21-9-8-19-18-7-6-16-14-17(27)10-12-25(16,4)20(18)11-13-26(19,21)5/h14,18-21H,6-13,15H2,1-5H3
InChI Key
VVOIQBFMTVCINR-UHFFFAOYSA-N
Formula
C26H38O4
SMILES
CC(C)(C)C(=O)OCC(=O)C1CCC2C3CCC4=CC(=O)CCC4(C)C3CCC12C
Molecular Weight1
414.58
CAS
808-48-0
Other Names
  • desoxycortone pivalate
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Physical Properties

Property Value Unit Source
Δfus 33.58 kJ/mol Joback Calculated Property
log10WS -5.70 Relay (1.0) Calculated Property
logPoct/wat 5.293 Crippen Calculated Property
McVol 340.040 ml/mol McGowan Calculated Property
Tfus 408.70 K Relay (1.0) Calculated Property

Cheméo can also estimate Normal Boiling Point Temperature, 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 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 [1290.78; 1499.40] J/mol×K [1014.75; 1261.79] Show Hide
Cp,gas 1290.78 J/mol×K 1014.75 Joback Calculated Property
Cp,gas 1321.63 J/mol×K 1055.92 Joback Calculated Property
Cp,gas 1353.51 J/mol×K 1097.10 Joback Calculated Property
Cp,gas 1386.83 J/mol×K 1138.27 Joback Calculated Property
Cp,gas 1421.98 J/mol×K 1179.44 Joback Calculated Property
Cp,gas 1459.37 J/mol×K 1220.61 Joback Calculated Property
Cp,gas 1499.40 J/mol×K 1261.79 Joback Calculated Property

Similar Compounds

Desoxycorticosterone Acetate. Deoxycorticosterone. 17beta-Acetoxy-10-isoandrost-4-en-3-one. Pregn-4-ene-3,20-dione, 11«alpha»-hydroxy-, acetate. 11«alpha»-Hydroxyprogesterone, TFA. Corticosterone, bis(pentafluoropropionate). 11.alpha.-hydroxyprogesterone, formate. 11.alpha.-Hydroxyprogesterone, methyl ether. 21-Hydroxyprogesterone, trimethylsilyl ether. Pregn-4-ene-3,20-dione, 11-hydroxy-, (11«alpha»)-. 17«alpha»,21-Dihydroxypregn-4-en-3,20-dione, 17,21-anhydro (oxetanone). Corticosterone. Pregn-4-ene-3,20-dione, 19,21-dihydroxy-. Hydroxyprogesterone Caproate. Aldosterone.

Find more compounds similar to 11-Deoxycorticosterone, pivalate.

Sources

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