Chemical Properties of Pregn-4-en-3-one, 20-hydroxy-, (20R)- (CAS 145-15-3)

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

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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?/m0/s1
InChI Key
RWBRUCCWZPSBFC-WWRIRWJESA-N
Formula
C21H32O2
SMILES
CC(O)C1CCC2C3CCC4=CC(=O)CCC4(C)C3CCC12C
Molecular Weight1
316.48
CAS
145-15-3
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
Δf 40.52 kJ/mol Joback Calculated Property
Δfgas -475.47 kJ/mol Joback Calculated Property
Δfus 22.64 kJ/mol Joback Calculated Property
Δvap 81.42 kJ/mol Joback Calculated Property
log10WS -5.25 Crippen Calculated Property
logPoct/wat 4.515 Crippen Calculated Property
McVol 266.450 ml/mol McGowan Calculated Property
Pc 1723.16 kPa Joback Calculated Property
Tboil 883.03 K Joback Calculated Property
Tc 1116.78 K Joback Calculated Property
Tfus 547.23 K Joback Calculated Property
Vc 1.000 m3/kmol Joback Calculated Property

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)-. Androst-4-en-3-one, 17-hydroxy-, (17«alpha»)-. Testosterone. 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. Calusterone. 17-epi-Bolasterone. Bolasterone. 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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