17-.beta.-Hydroxy-5.alpha.-androstan-3-one Diphenyl phosphate
Compound with spectra: 2 NMR, and 1 MS (GC)
| SpectraBase Compound ID | 4k0BFFHyopU |
|---|---|
| InChI | InChI=1S/C31H39O5P/c1-30-19-17-23(32)21-22(30)13-14-26-27-15-16-29(31(27,2)20-18-28(26)30)36-37(33,34-24-9-5-3-6-10-24)35-25-11-7-4-8-12-25/h3-12,22,26-29H,13-21H2,1-2H3/t22-,26-,27-,28-,29-,30-,31-/m0/s1 |
| InChIKey | KREVWTOITIDWGI-FKVQNEAASA-N |
| Mol Weight | 522.6 g/mol |
| Molecular Formula | C31H39O5P |
| Exact Mass | 522.253511 g/mol |
| Enantiomer InChIKey | KREVWTOITIDWGI-DPEJRGBQSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | F-68-5216-21 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
Methyloxime, t-butyldimethylsilyl derivative of 5.alpha.-Dihydroepitestosterone
Methyloxime, t-butyldimethylsilyl derivative of 5.alpha.-Dihydrotestosterone
5α-Pregnan-3,20-dione 20-ethyleneketal
5.beta.-Androstan-3-one, 17.beta.,19-dihydroxy-, diacetate
20β,21-(isopropylidenedioxy)-5β-pregnan-3-one
20β,21-dihydroxy-5β-pregnan-3-one, cyclic carbonate
20β,21-dihydroxy-5α-pregnan-3-one, cyclic carbonate
5α-Androstan-2α-bromo-17β-ol-3-one acetate
3,20-Dioxo-5β-pregnan-21-al, 21-(dimethyl acetal)
| Title | Journal or Book | Year |
|---|---|---|
| An Improved Method for Lewis Acid Catalyzed Phosphoryl Transfer with Ti(t-BuO)4 | The Journal of Organic Chemistry | 2003 |
Wiley Registry of Mass Spectral Data 12th Edition
Author: Wiley
The foundation library for any analytical laboratory running mass spectrometry, the Wiley Registry provides the broadest coverage available in any mass spectral library. Learn more.