In a comparative study of aromatic fluorodenitration with Potassium fluoride, in several dipolar aprotic solvents, a much faster reaction rate was observed with DMSO or tetramethylene sulfoxide than with the more commonly used Sulfolane.
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Applications
In a comparative study of aromatic fluorodenitration with Potassium fluoride, in several dipolar aprotic solvents, a much faster reaction rate was observed with DMSO or tetramethylene sulfoxide than with the more commonly used Sulfolane.
Solubility
Fully miscible in water.
Notes
Keep container tightly closed. Store away from oxidizing agents.
RUO – Research Use Only
General References:
- Philippe Renaud.; Nadira Moufid.; Lung Huang Kuo.; Dennis P. Curran. Altering the Stereochemistry of Allylation Reactions of Cyclic .alpha.-Sulfinyl Radicals: Effects of Solvents and Lewis Acids. J. Org. Chem. 1994, 59, (13), 3547-3552.
- Songping Wu.; Guobang Gu. Extraction of gold, palladium, and platinum from acidic media with cyclic sulfoxide derivative. Journal of University of Science and Technology Beijing, Mineral, Metallurgy, Material. 2007, 14, (2), 107-111.
- In a comparative study of aromatic fluorodenitration with Potassium fluoride, 14130 in several dipolar aprotic solvents, a much faster reaction rate was observed with DMSO or tetramethylene sulfoxide than with the more commonly used Sulfolane, A13466: J. Fluorine Chem., 35, 591 (1987).