Chemical Properties of (20S)-3«beta»-Acetoxy-29-(trimethylsilyloxy)lupane

(20S)-3«beta»-Acetoxy-29-(trimethylsilyloxy)lupane

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InChI
InChI=1S/C35H62O3Si/c1-23(22-37-39(9,10)11)25-14-17-32(5)20-21-34(7)26(30(25)32)12-13-28-33(6)18-16-29(38-24(2)36)31(3,4)27(33)15-19-35(28,34)8/h23,25-30H,12-22H2,1-11H3/t23-,25+,26?,27?,28?,29+,30?,32-,33+,34-,35-/m0/s1
InChI Key
CCMGLYUPVIXBBE-QDBTZTPFSA-N
Formula
C35H62O3Si
SMILES
CC(=O)OC1CCC2(C)C(CCC3(C)C2CCC2C4C(C(C)CO[Si](C)(C)C)CCC4(C)CCC23C)C1(C)C
Molecular Weight1
558.95
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Physical Properties

Property Value Unit Source
log10WS -7.40 Crippen Calculated Property
logPoct/wat 9.507 Crippen Calculated Property
Inp [3660.00; 3660.00]   Show Hide
Inp 3660.00 NIST
Inp 3660.00 NIST

Similar Compounds

(20R)-3«beta»-Acetoxy-29-(trimethylsilyloxy)lupane. 3«beta»-Acetoxy-20-(trimethylsilyloxy)lupane. 16«alpha», 17-H2(OH)2 GA9 methyl ester TMS ether. 3«beta»-Acetoxy-30-(trimethylsilyloxy)lup-20(29)-ene. Homocholic acid, acetate-methyl ester. Cholan-24-oic acid, 3,7,12-tris(acetyloxy)-, methyl ester, (3«alpha»,5«beta»,7«beta»,12«alpha»)-. 3«alpha»,7«beta»,12«beta»-Trihydroxy-5«beta»-cholanoic acid, acetate-methyl ester. 3«alpha»,7«alpha»,12«beta»-Trihydroxy-5«beta»-cholanoic acid, acetate-methyl ester. Cholan-24-oic acid, 3,7,12-tris(acetyloxy)-, methyl ester, (3«alpha»,5«beta»,7«alpha»,12«alpha»)-. 16«alpha», 17-H2-17-OH GA20 methyl ester TMS ether. 16«beta», 17-H2-17-OH GA20 methyl ester TMS ether. Oxandrolone, 17-TMS. Norcholic acid, acetate-methyl ester. 3«beta»-Hydroxy-7«beta»-methoxycholanic acid, methyl ester, TMS. 3«beta»-Hydroxy-7«alpha»-methoxycholanic acid, methyl ester, TMS.

Find more compounds similar to (20S)-3«beta»-Acetoxy-29-(trimethylsilyloxy)lupane.

Sources

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