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Potassium thioacetate is used for palladium mediated coupling with aryl halides and triflates leading to S-arylthioacetates and derivatives. It is also used as a reagent in the conversion of halides to thiols.
Reagent for the conversion of halides and sulfonates to thiols via the thiol acetates, thus avoiding the problem of sulfide formation: J. Chem. Soc., 579 (1950).
Ortega, P.; Gómez, R.; de la Mata, F. J. Thiol ended carbosilane dendrimers. A multivalent platform for the binding of molecules of biological interest. Tetrahedron Lett. 2015, 56 (38), 5299-5302.
Zhao, J.; Wang, C.; Zhao, P.; Wen, X.; Lin, C. Bioreducible dextran-polyethylenimine conjugates regulate transgene expression distribution in vivo. J. Mater. Chem. B 2015, 3 (8), 1529-1536.
Hazard Statements: H315-H319-H335
Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation.
Precautionary Statements: P261-P280a-P305+P351+P338-P304+P340-P405-P501a
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.