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Ethyl trifluoropyruvate acts as a building block in synthetic chemistry for the synthesis of fluorine containing compounds. It is also used as a reagent for the preparation of potential biologically active compounds like highly enantioselective organocatalytic hydroxyalkylation of indoles.
Li, K.; Zhao, X. M.; Yang, F. L.; Hou, X. H.; Xu, Y.; Guo, Y. C.; Hao, X. Q.; Song, M. P. Catalyst-free Friedel-Crafts hydroxyalkylation of imidazo[1,2-alpha]pyridines with ethyl trifluoropyruvate. RSC Adv. 2015, 5 (110), 90478-90481.
Montesinos-Magraner, M.; Vila, C.; Blay, G.; Fernández, I.; Muioz, M. C.; Pedro, J. R. Organocatalytic Enantioselective Friedel-Crafts Alkylation of 1-Naphthol Derivatives and Activated Phenols with Ethyl Trifluoropyruvate. Adv. Synth. Catal. 2015, 357 (14-15), 3047-3051.
Gefahrenhinweise (EU): H226-H315-H319-H335
Flammable liquid and vapour. Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation.
Keep away from heat/sparks/open flames/hot surfaces. - No smoking. Avoid breathing dust/fume/gas/mist/vapours/spray. IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.