(E)-4-keto-3-methyl-but-2-enoic acid 2,2,2-trifluoroethyl ester
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 8JDaXj93ahH |
|---|---|
| InChI | InChI=1S/C7H7F3O3/c1-5(3-11)2-6(12)13-4-7(8,9)10/h2-3H,4H2,1H3/b5-2+ |
| InChIKey | MNEKZAMCGOVTIF-GORDUTHDSA-N |
| Mol Weight | 196.13 g/mol |
| Molecular Formula | C7H7F3O3 |
| Exact Mass | 196.034729 g/mol |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
NZSUTQWXDVADEV-UHFFFAOYSA-N
2',2',2'-TRIFLUOROETHYL-3-OXO-BUTANOATE;ENOL-TAUTOMER
2,2,2-TRIFLUOROETHYL-3-ISOPROPYLACRYLATE;TRIFLUOROETHYL-4-METHYLPENT-2-ENOATE
2,2,2-trifluoroethyl (Z)-2-methylbut-2-enoate
Ethyl [(E,E)-5-Iodo-3-methylpenta-2,4-dienoate
Norsocryl trifluoroethyl methacrylate (MATRIFE)
5-keto-2H-furan-3-carbaldehyde
(E)-2,2,2-Trifluoroethyl 2-bromobut-2-enoate
Ethyl (2E,4E)-5-formyl-3-methylpenta-2,4-dienoate
3-acetylcrotonic acid, ethyl ester
| Title | Journal or Book | Year |
|---|---|---|
| Application of Chiral Cationic Catalysts to Several Classical Syntheses of Racemic Natural Products Transforms Them into Highly Enantioselective Pathways | Journal of the American Chemical Society | 2004 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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