Chemical Properties of Pregn-4-en-3-one, 20-hydroxy-, (20r)-

Pregn-4-en-3-one, 20-hydroxy-, (20r)-

InChI
InChI=1S/C21H32O2/c1-13(22)17-6-7-18-16-5-4-14-12-15(23)8-10-20(14,2)19(16)9-11-21(17,18)3/h12-13,16-19,22H,4-11H2,1-3H3/t13-,16?,17?,18?,19?,20?,21?/m1/s1
InChI Key
RWBRUCCWZPSBFC-WWRIRWJESA-N
Formula
C21H32O2
SMILES
C[C@@H](O)C1CCC2C3CCC4=CC(=O)CCC4(C)C3CCC21C
Molecular Weight1
316.48
Other Names
  • Pregn-4-en-3-one, 20«beta»-hydroxy-
  • Progesterol-20«beta»
  • 20«beta»-Dihydroprogesterone
  • 20«beta»-Hydroxydihydroprogesterone
  • 20«beta»-Hydroxyprogesterone
  • 20«beta»-Progerol
  • 20-«beta»-Hydroxypregn-4-en-3-one
  • 4-Pregnen-20«beta»-ol-3-one
  • 20-Hydroxypregn-4-en-3-one, (20«beta»)-
  • (20R)-20-hydroxypregn-4-en-3-one
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Physical Properties

Property Value Unit Source
Δfus 22.64 kJ/mol Joback Calculated Property
log10WS -4.53 Relay (1.0) Calculated Property
logPoct/wat 4.515 Crippen Calculated Property
McVol 266.450 ml/mol McGowan Calculated Property
Tfus 461.44 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 [964.98; 1127.47] J/mol×K [883.03; 1116.78] Show Hide
Cp,gas 964.98 J/mol×K 883.03 Joback Calculated Property
Cp,gas 990.52 J/mol×K 921.99 Joback Calculated Property
Cp,gas 1016.25 J/mol×K 960.95 Joback Calculated Property
Cp,gas 1042.50 J/mol×K 999.91 Joback Calculated Property
Cp,gas 1069.57 J/mol×K 1038.86 Joback Calculated Property
Cp,gas 1097.78 J/mol×K 1077.82 Joback Calculated Property
Cp,gas 1127.47 J/mol×K 1116.78 Joback Calculated Property

Similar Compounds

Pregn-4-en-3-one, 20-hydroxy-, (20S)-. Testosterone. Androst-4-en-3-one, 17-hydroxy-, (17«alpha»)-. Nandrolone. Pregn-4-ene-3,20-dione, 11-hydroxy-, (11«alpha»)-. Androsten-17-(beta)-ol-3-one, 17(alpha)-methyl-delta^4-. 17-epi-Methyltestosterone. 17«alpha»-Methyltestosterone. 17-epi-Bolasterone. Bolasterone. Calusterone. Methenolone. 11«alpha»-Hydroxy-17«alpha»-methyl testosterone. Androst-4-ene-3,17-dione, 11-hydroxy-, (11«beta»)-. Corticosterone.

Find more compounds similar to Pregn-4-en-3-one, 20-hydroxy-, (20r)-.

Sources

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