Chemical Properties of Oxymesterone (CAS 145-12-0)

Oxymesterone

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InChI
InChI=1S/C20H30O3/c1-18-9-8-16(21)17(22)15(18)5-4-12-13(18)6-10-19(2)14(12)7-11-20(19,3)23/h12-14,22-23H,4-11H2,1-3H3/t12?,13?,14?,18?,19?,20-/m1/s1
InChI Key
RXXBBHGCAXVBES-XPUDHZTDSA-N
Formula
C20H30O3
SMILES
CC12CCC(=O)C(O)=C1CCC1C2CCC2(C)C1CCC2(C)O
Molecular Weight1
318.45
CAS
145-12-0
Other Names
  • Androst-4-en-3-one, 4,17-dihydroxy-17-methyl-, (17«beta»)-
  • Androst-4-en-3-one, 4,17«beta»-dihydroxy-17-methyl-
  • Aranabol
  • Oranabol
  • Testosterone, 4-hydroxy-17-methyl-
  • 4-Hydroxy-17«alpha»-methyltestosterone
  • 4-Hydroxy-17-methyltestosterone
  • 4,17«beta»-Dihydroxy-17-methylandrost-4-en-3-one
  • 4,17«beta»-Dihydroxy-17«alpha»-methylandrost-4-en-3-one
  • Anamidol
  • Oxymestrone
  • Theranabol
  • 4,17-Dihydroxy-17-methylandrost-4-en-3-one
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Physical Properties

Property Value Unit Source
Δf -117.40 kJ/mol Joback Calculated Property
Δfgas -598.01 kJ/mol Joback Calculated Property
Δfus 20.97 kJ/mol Joback Calculated Property
Δvap 95.78 kJ/mol Joback Calculated Property
log10WS -4.89 Crippen Calculated Property
logPoct/wat 4.155 Crippen Calculated Property
McVol 258.230 ml/mol McGowan Calculated Property
Pc 2068.00 kPa Joback Calculated Property
Inp [2703.00; 2766.50]   Show Hide
Inp 2766.50 NIST
Inp 2703.00 NIST
Tboil 957.99 K Joback Calculated Property
Tc 1189.14 K Joback Calculated Property
Tfus 648.20 K Joback Calculated Property
Vc 0.967 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [981.42; 1193.26] J/mol×K [957.99; 1189.14] Show Hide
Cp,gas 981.42 J/mol×K 957.99 Joback Calculated Property
Cp,gas 1010.66 J/mol×K 996.52 Joback Calculated Property
Cp,gas 1041.79 J/mol×K 1035.04 Joback Calculated Property
Cp,gas 1075.21 J/mol×K 1073.57 Joback Calculated Property
Cp,gas 1111.32 J/mol×K 1112.09 Joback Calculated Property
Cp,gas 1150.54 J/mol×K 1150.62 Joback Calculated Property
Cp,gas 1193.26 J/mol×K 1189.14 Joback Calculated Property

Similar Compounds

4-Androsten-3-one, 4,17beta-dihydroxy-17alpha-methyl-. 17-epi-Oxamesterone. A-norandrost-3(5)-en-2-one, 3,17-dihydroxy-. 11«alpha»-Hydroxy-17«alpha»-methyl testosterone. 17«alpha»-Methyltestosterone. Androsten-17-(beta)-ol-3-one, 17(alpha)-methyl-delta^4-. 17-epi-Methyltestosterone. 17-epi-Bolasterone. Calusterone. Bolasterone. Ethisterone. Ethisterone. 17«alpha»-Hydroxyprogesterone. 17«alpha»-Hydroxyprogesterone. Norethisterone.

Find more compounds similar to Oxymesterone.

Sources

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