Chemical Properties of 5.alpha.-Androstane-3.beta.,17.beta.-diol, dimethyl ether

5.alpha.-Androstane-3.beta.,17.beta.-diol, dimethyl ether

InChI
InChI=1S/C21H36O2/c1-20-11-9-15(22-3)13-14(20)5-6-16-17-7-8-19(23-4)21(17,2)12-10-18(16)20/h14-19H,5-13H2,1-4H3
InChI Key
AQOCBVOXXCEOLR-UHFFFAOYSA-N
Formula
C21H36O2
SMILES
COC1CCC2(C)C(CCC3C2CCC2(C)C(OC)CCC32)C1
Molecular Weight1
320.52
Other Names
  • (3«beta»,5«alpha»,17«beta»)-3,17-Dimethoxyandrostane
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Physical Properties

Property Value Unit Source
Δfus 26.25 kJ/mol Joback Calculated Property
log10WS -5.58 Relay (1.0) Calculated Property
logPoct/wat 5.059 Crippen Calculated Property
McVol 275.050 ml/mol McGowan Calculated Property
Tfus 370.22 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 [934.14; 1096.78] J/mol×K [754.83; 982.84] Show Hide
Cp,gas 934.14 J/mol×K 754.83 Joback Calculated Property
Cp,gas 962.78 J/mol×K 792.83 Joback Calculated Property
Cp,gas 990.43 J/mol×K 830.83 Joback Calculated Property
Cp,gas 1017.38 J/mol×K 868.83 Joback Calculated Property
Cp,gas 1043.89 J/mol×K 906.84 Joback Calculated Property
Cp,gas 1070.27 J/mol×K 944.84 Joback Calculated Property
Cp,gas 1096.78 J/mol×K 982.84 Joback Calculated Property

Similar Compounds

BICYCLO[2.2.1]HEPTANE, 2-METHOXY-1,7,7-TRIMETHYL-. bornyl methyl ether. Khusian-2-yl methyl ether. Isobornyl formate. Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, formate, endo-. 5«beta»-Cholestan-3«alpha»-ol, methyl ether. Coprostan-3-ol, methyl ether. 4«alpha»-Methoxy-1,1,2«alpha»,5-tetramethyldecahydrocyclopenta[cd]indene. Androstan-17-ol, acetate, (5«alpha»,17«beta»)-. Ambrox. Tricyclo[4.3.1.1(2,5)]undecane, 10-methoxy-, stereoisomer. Bornyl acetate. Isobornyl acetate. Acetic acid, 1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester. Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl, acetate.

Find more compounds similar to 5.alpha.-Androstane-3.beta.,17.beta.-diol, dimethyl ether.

Sources

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