Chemical Properties of 21-Hydroxyprogesterone, tert-butyldimethylsilyl ether

21-Hydroxyprogesterone, tert-butyldimethylsilyl ether

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InChI
InChI=1S/C27H44O3Si/c1-25(2,3)31(6,7)30-17-24(29)23-11-10-21-20-9-8-18-16-19(28)12-14-26(18,4)22(20)13-15-27(21,23)5/h16,20-23H,8-15,17H2,1-7H3
InChI Key
XFKHARHPUCVJDK-UHFFFAOYSA-N
Formula
C27H44O3Si
SMILES
CC12CCC(=O)C=C1CCC1C2CCC2(C)C(C(=O)CO[Si](C)(C)C(C)(C)C)CCC12
Molecular Weight1
444.72
Other Names
  • 21-Hydroxyprogesterone, tbdms derivative
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Physical Properties

Property Value Unit Source
log10WS -4.81 Crippen Calculated Property
logPoct/wat 6.725 Crippen Calculated Property
Inp [3403.30; 3403.30]   Show Hide
Inp 3403.30 NIST
Inp 3403.30 NIST

Similar Compounds

21-Hydroxyprogesterone, trimethylsilyl ether. Corticosterone, bis(trimethylsilyl) ether. Testosterone, 17-O-(t-butyldimethylsilyl)-. Epitestosterone, tert-butyldimethylsilyl ether. 11«alpha»-Hydroxyprogesterone, trimethylsilyl ether. Pregnenolone, 3-dimethyl(t-butyl)silyl ether. Dehydroepiandrosterone, TBDMSi (3-O). trans-Dehydroandrosterone, tert-butyldimethylsilyl ether. Deoxycorticosterone. 17«alpha»-Hydroxyprogesterone, trimethylsilyl ether. 5-Pregnen-3«beta»,20«alpha»-diol, TBDMS. 11-Dehydrocorticosterone, MO-TMS. Desoxycorticosterone Acetate. 11-Deoxycorticosterone, pivalate. Pregn-4-ene-3,20-dione, 19,21-dihydroxy-.

Find more compounds similar to 21-Hydroxyprogesterone, tert-butyldimethylsilyl ether.

Sources

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