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It is employed as a reactant involved in radical coupling, synthesis of organosoluble zirconium phosphonate nanocomposites, click-chemistry, asymmetric epoxidation of unfunctionalized olefins, Negishi alkyl-aryl cross-coupling, and in synthesis of hydrolytically stable phosphonic acids for use as dental adhesives.
Taotao Chen, et al. Organosoluble zirconium phosphonate nanocomposites and their supported chiral ruthenium catalysts: the first example of homogenization of inorganic-supported catalyst in asymmetric hydrogenation.Dalton Trans.201140(13), 3325-3335.
A. H. Ford-Moore and J. Howarth Williams. The reaction between trialkyl phosphites and alkyl halides.J. Chem. Soc.,19471465-1467.
Gefahrenhinweise (EU): H315-H319-H335
Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation.
Avoid breathing dust/fume/gas/mist/vapours/spray. Wear protective gloves and eye/face protection. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.