3-(Cyclopentyloxy)-4-methoxybenzaldehyde
Compound with spectra: 1 NMR, and 1 MS (GC)
| SpectraBase Compound ID | KQxCZtX6X3t |
|---|---|
| InChI | InChI=1S/C13H16O3/c1-15-12-7-6-10(9-14)8-13(12)16-11-4-2-3-5-11/h6-9,11H,2-5H2,1H3 |
| InChIKey | FZFWPURYSWKIRT-UHFFFAOYSA-N |
| Mol Weight | 220.27 g/mol |
| Molecular Formula | C13H16O3 |
| Exact Mass | 220.109944 g/mol |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | F-62-4914-20 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
5-Formyl-2-methoxyphenyl propionate
3,4-BIS-(HEXYLOXY)-BENZALDEHYDE
3-Hexyloxy-4-(2'-hydroxyethoxy)-benzaldehyde
3,4-BIS-(HEXADECYLOXY)-BENZALDEHYDE
3-(Benzyloxy)-4-methoxybenzaldehyde
4-Methoxy-3-[(4-methylbenzyl)oxy]benzaldehyde
tert-Butyl (E)-3-(5-Formyl-2-methoxyphenoxy)prop-2-enoate
3-Isopropoxy-4-methoxybenzamide
4-formyl-2-methoxyphenyl propionate
3-ethoxy-4-[2-(4-morpholinyl)ethoxy]benzaldehyde
| Title | Journal or Book | Year |
|---|---|---|
| Enantioselective Michael Additions of Nitromethane by a Catalytic Double Activation Method Using Chiral Lewis Acid and Achiral Amine Catalysts | Journal of the American Chemical Society | 2002 |
Wiley Registry of Mass Spectral Data 12th Edition
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Wiley Registry of Mass Spectral Data 2023
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.