Chemical Properties of 17-epi-Bolasterone, 17-TMS

17-epi-Bolasterone, 17-TMS

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InChI
InChI=1S/C24H40O2Si/c1-16-14-17-15-18(25)8-11-22(17,2)19-9-12-23(3)20(21(16)19)10-13-24(23,4)26-27(5,6)7/h15-16,19-21H,8-14H2,1-7H3/t16-,19?,20?,21?,22?,23?,24-/m0/s1
InChI Key
YODBBXQVBBUISJ-LJJFCTPYSA-N
Formula
C24H40O2Si
SMILES
CC1CC2=CC(=O)CCC2(C)C2CCC3(C)C(CCC3(C)O[Si](C)(C)C)C12
Molecular Weight1
388.66
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Physical Properties

Property Value Unit Source
ω 0.5527 Relay (... Calculated Property
Δf 24.15 kJ/mol Relay (... Calculated Property ⚠️
Δfgas -621.57 kJ/mol Relay (... Calculated Property
Δvap 104.37 kJ/mol Relay (... Calculated Property
IE 8.75 eV Relay (... Calculated Property
log10WS -5.21 Relay (... Calculated Property
logPoct/wat 6.375 Crippen Calculated Property
Pc 775.05 kPa Relay (... Calculated Property ⚠️
Inp [2731.00; 2731.00]   Show Hide
Inp 2731.00 NIST
Inp 2731.00 NIST
Tboil 661.51 K Relay (... Calculated Property
Tc 928.52 K Relay (... Calculated Property
Tfus 412.81 K Relay (... Calculated Property
Vc 1.225 m3/kmol Relay (... Calculated Property

Similar Compounds

Bolasterone, TMS. Methyltestosterone, 17-TMS. 17-epi-Methyltestosterone, 17-TMS. 19-Nor-17«alpha»-pregn-4-en-3-one, 17-(trimethylsiloxy)-. 20«alpha»-Hydroxy-4-cholesten-3-one, TMS. 17«alpha»-Hydroxyprogesterone, trimethylsilyl ether. Silandrone. Androst-4-en-3-one, 17-[(trimethylsilyl)oxy]-, (17«alpha»)-. 22-Hydroxy-4-cholesten-3-one, TMS. 24-Hydroxy-4-cholesten-3-one, TMS. 17-epi-Methandienone, 17-TMS. 17«alpha»-Methyl-17«beta»-hydroxy-1,4-androstadien-3-one, trimethylsilyl deriv.. 17-Epimetandienone (Androst-1,4-dien-17B-methyl-17A-ol-3-one), TMS. Methenolone, trimethylsilyl ether. Testosterone, 17-O-(t-butyldimethylsilyl)-.

Find more compounds similar to 17-epi-Bolasterone, 17-TMS.

Sources

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