4-Toluenesulfonyl chloride (p-toluenesulfonyl chloride, toluene-p-sulfonyl chloride) is an organic compound with the formula CH3C6H4SO2Cl. This white, malodorous solid is a reagent widely used in organic synthesis. Abbreviated TsCl or TosCl, it is a derivative of toluene and contains a sulfonyl chloride (−SO2Cl) … See more In characteristic manner, TsCl converts alcohols (abbreviated ROH) into the corresponding toluenesulfonate esters, or tosyl derivatives ("tosylates"): CH3C6H4SO2Cl + ROH → CH3C6H4SO2OR + … See more Being a widely available reagent, TsCl has been heavily examined from the perspective of reactivity. It is used in dehydrations to make nitriles, isocyanides and diimides. In an unusual reaction focusing on the sulfur center, zinc reduces TsCl to the sulfinate, … See more This reagent is inexpensively available for laboratory use. It is a by-product from the production of ortho-toluenesulfonyl chloride (a precursor … See more Tosyl chloride is considered to be a toxic and corrosive substance. See more Web2024 Minnesota Cup. Register today for Minnesota’s marquee event! Open to 11U-19U Boys & Girls; 13U+ winners advance to US Club Soccer national events.
The Senior Citizens League Welcome to TSCL
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WebPyridine C5H5N CID 1049 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards ... WebMar 10, 2015 · All About Tosylates and Mesylates. By themselves, alcohols are poor leaving groups since the hydroxide ion (HO-) is a strong base; The OH group can be converted into … Web4-Toluenesulfonyl chloride. Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Tosyl chloride or 4-Toluenesulfonyl … simply red atlas arena