Chemical Properties of 17-«alpha»-Hydroxy-17-«beta»-methyl-5-«beta»-androst-1-en-3-one, 17-TMS

17-«alpha»-Hydroxy-17-«beta»-methyl-5-«beta»-androst-1-en-3-one, 17-TMS

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InChI
InChI=1S/C23H38O2Si/c1-21-12-9-17(24)15-16(21)7-8-18-19(21)10-13-22(2)20(18)11-14-23(22,3)25-26(4,5)6/h9,12,16,18-20H,7-8,10-11,13-15H2,1-6H3/t16-,18?,19?,20?,21?,22?,23-/m0/s1
InChI Key
LVNZBAUCPORGGO-MQOPPOBTSA-N
Formula
C23H38O2Si
SMILES
CC12C=CC(=O)CC1CCC1C2CCC2(C)C1CCC2(C)O[Si](C)(C)C
Molecular Weight1
374.63
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Physical Properties

Property Value Unit Source
log10WS -3.96 Crippen Calculated Property
logPoct/wat 5.984 Crippen Calculated Property
Inp [2556.00; 2556.00]   Show Hide
Inp 2556.00 NIST
Inp 2556.00 NIST

Similar Compounds

17-«beta»-Hydroxy-17-«alpha»-methyl-5-«beta»-androst-1-en-3-one, 17-TMS. Methyltestosterone, 17-TMS. 17-epi-Methyltestosterone, 17-TMS. 17-epi-Bolasterone, 17-TMS. Bolasterone, TMS. 19-Nor-17«alpha»-pregn-4-en-3-one, 17-(trimethylsiloxy)-. 17«alpha»-Hydroxyprogesterone, trimethylsilyl ether. Methenolone, trimethylsilyl ether. 20«alpha»-Hydroxy-4-cholesten-3-one, TMS. 17-Epimetandienone (Androst-1,4-dien-17B-methyl-17A-ol-3-one), TMS. 17«alpha»-Methyl-17«beta»-hydroxy-1,4-androstadien-3-one, trimethylsilyl deriv.. 17-epi-Methandienone, 17-TMS. Androst-4-en-3-one, 17-[(trimethylsilyl)oxy]-, (17«alpha»)-. Silandrone. 17-«beta»-Hydroxy-17-«alpha»-methyl-5-«beta»-androst-1-en-3-one.

Find more compounds similar to 17-«alpha»-Hydroxy-17-«beta»-methyl-5-«beta»-androst-1-en-3-one, 17-TMS.

Sources

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