Lanosteryl acetate
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 5HnpMYBwJSd |
|---|---|
| InChI | InChI=1S/C32H52O2/c1-21(2)11-10-12-22(3)24-15-19-32(9)26-13-14-27-29(5,6)28(34-23(4)33)17-18-30(27,7)25(26)16-20-31(24,32)8/h11,22,24,27-28H,10,12-20H2,1-9H3/t22?,24-,27+,28+,30-,31-,32+/m1/s1 |
| InChIKey | BQPPJGMMIYJVBR-ZXLAETICSA-N |
| Mol Weight | 468.8 g/mol |
| Molecular Formula | C32H52O2 |
| Exact Mass | 468.396731 g/mol |
| Enantiomer InChIKey | BQPPJGMMIYJVBR-PMPFJDKLSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3;0.03M |
Lanosteryl acetate
22,22-DIDEUTERO-LANOSTA-8,24-DIEN-3-YL ACETATE
TIRUCALLA-8,24-DIEN-3-BETA-OL-ACETATE;TIRUCALLOL-ACETATE
Lanosta-8,24-dien-3-yl acetate
3-ACETOLANOSTEROL;4,4,14-ALPHA-TRIMETHYL-5-ALPHA-CHOLESTA-8,24-DIEN-3-ACETYL
21-DEUTERO-LANOSTA-8,24-DIEN-3-YL ACETATE
EUPHA-8,24-DIEN-3-BETA-OL-ACETATE;EUPHOL-ACETATE
Euphol acetate
Lanosta-8,24-dien-3-ol, acetate, (3.beta.)-
| Title | Journal or Book | Year |
|---|---|---|
| Phenylalanine 445 within Oxidosqualene−Lanosterol Cyclase from Saccharomyces cerevisiae Influences C-Ring Cyclization and Deprotonation Reactions | Organic Letters | 2006 |
This compound is available in the following databases:
Mass Spectra of Designer Drugs 2024
Author: Peter Rösner
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