Chemical Properties of Methyltestosterone, HFB

Methyltestosterone, HFB

InChI
InChI=1S/C24H29F7O3/c1-19-9-6-14(32)12-13(19)4-5-15-16(19)7-10-20(2)17(15)8-11-21(20,3)34-18(33)22(25,26)23(27,28)24(29,30)31/h12,15-17H,4-11H2,1-3H3/t15?,16?,17?,19-,20-,21+/m0/s1
InChI Key
FXQFIJSPYKJFSH-XXYOTYRBSA-N
Formula
C24H29F7O3
SMILES
C[C@]12CCC(=O)C=C1CCC1C2CC[C@@]2(C)C1CC[C@@]2(C)OC(=O)C(F)(F)C(F)(F)C(F)(F)F
Molecular Weight1
498.48
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Physical Properties

Property Value Unit Source
ΔfusH° 27.23 kJ/mol Joback Calculated Property
log10WS -6.89 Relay (1.0) Calculated Property
logPoct/wat 6.653 Crippen Calculated Property
McVol 322.680 ml/mol McGowan Calculated Property
Inp 2272.00 NIST
Tfus 392.40 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 [1175.54; 1359.22] J/mol×K [903.79; 1124.45] Show Hide
Cp,gas 1175.54 J/mol×K 903.79 Joback Calculated Property
Cp,gas 1202.11 J/mol×K 940.57 Joback Calculated Property
Cp,gas 1229.74 J/mol×K 977.34 Joback Calculated Property
Cp,gas 1258.83 J/mol×K 1014.12 Joback Calculated Property
Cp,gas 1289.83 J/mol×K 1050.89 Joback Calculated Property
Cp,gas 1323.15 J/mol×K 1087.67 Joback Calculated Property
Cp,gas 1359.22 J/mol×K 1124.45 Joback Calculated Property

Similar Compounds

Testosterone, HFB. Nortestosterone, HFB. methyltestosterone acetate. 5-«alpha»-Androst-9(11)-ene-3-«alpha»,17-«beta»-diol, HFB. 10A,12a-dimethyl-3,4,4a,5,6,9,10,10a,10b,11,12,12a-dodecahydro-2h-naphtho[2,1-f]chromene-2,8(4bh)-dione. Hydroxyprogesterone Caproate. 5-Androsten-3-«alpha»,17-«beta»-diol, HFB. 5-Androsten-3-«beta»,17-«beta»-diol, HFB. 5-Androsten-3-«beta»,17-«alpha»-diol, HFB. 5-Pregnen-3-«beta»,20-«alpha»-diol, HFB. 5-Pregnen-3-«beta»,20-«beta»-diol, HFB. Medroxyprogesterone Acetate. 17Alpha-acetoxy-6alpha-methyl-pregn-4-ene-3,20-dione. Testosterone acetate. Norethindrone Acetate.

Find more compounds similar to Methyltestosterone, HFB.

Sources

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