Chemical Properties of Corticosterone, bis(trimethylsilyl) ether

Corticosterone, bis(trimethylsilyl) ether

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InChI
InChI=1S/C27H46O4Si2/c1-26-14-13-19(28)15-18(26)9-10-20-21-11-12-22(23(29)17-30-32(3,4)5)27(21,2)16-24(25(20)26)31-33(6,7)8/h15,20-22,24-25H,9-14,16-17H2,1-8H3
InChI Key
GCLMSBAIDKDJJQ-UHFFFAOYSA-N
Formula
C27H46O4Si2
SMILES
CC12CCC(=O)C=C1CCC1C2C(O[Si](C)(C)C)CC2(C)C(C(=O)CO[Si](C)(C)C)CCC12
Molecular Weight1
490.82
Other Names
  • (11«beta»)-11,21-Bis[(trimethylsilyl)oxy]pregn-4-ene-3,20-dione
  • Corticosteron, 2tms derivative
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Physical Properties

Property Value Unit Source
log10WS -2.06 Crippen Calculated Property
logPoct/wat 6.385 Crippen Calculated Property
Inp [3867.40; 3867.40]   Show Hide
Inp 3867.40 NIST
Inp 3867.40 NIST

Similar Compounds

11«alpha»-Hydroxyprogesterone, trimethylsilyl ether. 20«beta»,21-Dihydroxypregn-4-en-3-one, 20,21-bis-TMS. 22-Hydroxy-4-cholesten-3-one, TMS. 11«alpha»-hydroxyprogesterone, formate. Androst-4-en-3-one, 17-[(trimethylsilyl)oxy]-, (17«alpha»)-. Silandrone. 3B,16A,20A-Trihydroxypregn-5-ene, tris-TMS. 3-«beta»,19-Dihydroxy-5-androsten-17-one, TMS. Cholest-5-en-7-one, 3-[(trimethylsilyl)oxy]-. 17«alpha»-Hydroxyprogesterone, trimethylsilyl ether. 24-Hydroxy-4-cholesten-3-one, TMS. Epitestosterone, tert-butyldimethylsilyl ether. Testosterone, 17-O-(t-butyldimethylsilyl)-. 11«alpha»-Hydroxyprogesterone, TFA. 11«alpha»-Hydroxyprogesterone, methyl ether.

Find more compounds similar to Corticosterone, bis(trimethylsilyl) ether.

Sources

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