(1R)-CYCLOHEX-3-ENECARBOXYLIC-ACID-2,2,2-TRIFLUORO-ETHYLESTER
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 32mjtULUjk7 |
|---|---|
| InChI | InChI=1S/C9H11F3O2/c10-9(11,12)6-14-8(13)7-4-2-1-3-5-7/h1-2,7H,3-6H2/t7-/m0/s1 |
| InChIKey | FWRKUOVBXXYWPW-ZETCQYMHSA-N |
| Mol Weight | 208.18 g/mol |
| Molecular Formula | C9H11F3O2 |
| Exact Mass | 208.071114 g/mol |
| Enantiomer InChIKey | FWRKUOVBXXYWPW-SSDOTTSWSA-N |
| Racemate InChIKey | FWRKUOVBXXYWPW-UHFFFAOYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
3-Cyclohexene-1-carboxylic acid, 2-hydroxy-ethyl ester
3-Cyclohexenecarboxylic acid, butyl ester
3-Cyclohexene-1-carboxylic acid, isobutyl ester
3-cyclohexene-1-carboxylic acid, isopropyl ester
3-Cyclohexene-1-carboxylic acid, tert-butyl ester
Cyclohexene-4-carboxylic acid trimethylsilyl ester
Ethyl 4-cyclooctene-1-carboxylate
Cyclobutanecarboxylic acid, 2,2,3,3-tetrafluoropropyl ester
4-Methyl-3-cyclohexene-1-carboxylic acid, methyl ester
| Title | Journal or Book | Year |
|---|---|---|
| Triflimide Activation of a Chiral Oxazaborolidine Leads to a More General Catalytic System for Enantioselective Diels−Alder Addition | Journal of the American Chemical Society | 2003 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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