Chemical Properties of 5Alpha-androstan-16beta-ylacetic acid lactone, 3beta,17beta-dihydroxy-

5Alpha-androstan-16beta-ylacetic acid lactone, 3beta,17beta-dihydroxy-

InChI
InChI=1S/C21H32O3/c1-20-7-5-14(22)11-13(20)3-4-15-16(20)6-8-21(2)17(15)9-12-10-18(23)24-19(12)21/h12-17,19,22H,3-11H2,1-2H3/t12-,13+,14+,15-,16+,17+,19+,20+,21+/m0/s1
InChI Key
TWLWASBVSWBNCK-JXURMTEMSA-N
Formula
C21H32O3
SMILES
CC12CCC(O)CC1CCC1C2CCC2(C)C1CC1CC(=O)OC12
Molecular Weight1
332.48
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Physical Properties

Property Value Unit Source
Δfus 33.59 kJ/mol Joback Calculated Property
log10WS -4.51 Relay (1.0) Calculated Property
logPoct/wat 3.932 Crippen Calculated Property
McVol 265.760 ml/mol McGowan Calculated Property
Tfus 463.64 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 [1022.23; 1197.24] J/mol×K [903.68; 1141.33] Show Hide
Cp,gas 1022.23 J/mol×K 903.68 Joback Calculated Property
Cp,gas 1049.39 J/mol×K 943.29 Joback Calculated Property
Cp,gas 1076.88 J/mol×K 982.90 Joback Calculated Property
Cp,gas 1105.05 J/mol×K 1022.50 Joback Calculated Property
Cp,gas 1134.27 J/mol×K 1062.11 Joback Calculated Property
Cp,gas 1164.88 J/mol×K 1101.72 Joback Calculated Property
Cp,gas 1197.24 J/mol×K 1141.33 Joback Calculated Property

Similar Compounds

5Beta-androstan-16beta-ylacetic acid lactone, 3beta,17beta-dihydroxy-. 3Beta-acetoxy-17beta-hydroxy-5alpha-androstan-16beta-ylacetic acid lactone. Acetic acid, (17beta-hydroxy-3-oxo-5beta-androstan-16-beta-yl)-, lactone. 5Alpha-androstone-3beta, 17beta-diol,16-ylacetic acid, 3,17-diacetate. 3-Oxa-a-nor-5alpha-androstan-2-one, 17-hydroxy-, acetate. 5-hydroxy-isobornyl butyrate. Isobornyl caprate. Isobornyl laureate. Bornyl hexanoate. Pentanoic acid, 1,7,7-trimethylbicyclo[2.2.1]hept-2-yl ester, endo-. 5«alpha»,17«alpha»-Dihydroepitestosterone tetradecanoate. 5«beta»,17«alpha»-Dihydroepitestosterone octadecanoate. 5«beta»,17«beta»-Dihydrotestosterone tetradecanoate. 5«alpha»,17«alpha»-Dihydroepitestosterone decanoate. 5«alpha»,17«beta»-Dihydrotestosterone dodecanoate.

Find more compounds similar to 5Alpha-androstan-16beta-ylacetic acid lactone, 3beta,17beta-dihydroxy-.

Sources

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