3-METHOXY-17A,17B-DIHOMOESTRA-1,3,5(10),16-TETRAEN-17B-BETA-OL
Compound with spectra: 1 NMR
| SpectraBase Compound ID | KFmLkztiLJ1 |
|---|---|
| InChI | InChI=1S/C21H28O2/c1-21-12-11-17-16-10-8-15(23-2)13-14(16)7-9-18(17)19(21)5-3-4-6-20(21)22/h3-4,8,10,13,17-20,22H,5-7,9,11-12H2,1-2H3/t17-,18-,19+,20+,21+/m1/s1 |
| InChIKey | WJPJZZLZFNMRME-MJCUULBUSA-N |
| Mol Weight | 312.45 g/mol |
| Molecular Formula | C21H28O2 |
| Exact Mass | 312.20893 g/mol |
| Enantiomer InChIKey | WJPJZZLZFNMRME-WRTQPQOASA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(1'S)-13-(1'-HYDROXYBUT-3'-ENYL)-3-METHOXY-13,17-SECO-ESTRA-1,2,5(10),16-TETRAENE
(1'R)-13-(1'-HYDROXYBUT-3'-ENYL)-3-METHOXY-13,17-SECO-ESTRA-1,2,5(10),16-TETRAENE
3-Methoxy-17a-hydroxy-(8a,9a,14B)-thiasteroid
(17.beta.)estra-1,3,5(10)triene-3-acetoxy-17-ol
17α-Estradiol 3-acetate
17β-Estradiol 3-acetate
3-OCTYLOXY-ESTRA-1,3,5(10)-TRIEN-17-BETA-OL
3-(Pivaloyloxy)estran-17.beta.-ol
Estradiol 3-(trimethylsilyl) ether
| Title | Journal or Book | Year |
|---|---|---|
| Increasing the amphiphilicity of an estradiol based steroid structure by Barbier-allylation – ring-closing metathesis – dihydroxylation sequence | Steroids | 2012 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
The KnowItAll NMR Spectral Library offers a comprehensive collection of NMR reference spectra, including NMR, CNMR, and XNMR, and covers a wide range of compounds including organics, polymers, monomers, metabolites, and more. Learn more.