toluenesulfonyl การใช้

• The closely related compound toluenesulfonyl chloride is often preferred analogue because it is a solid at room temperature and easier to handle.
• Esters of " N "-hydroxyphthalimide and activated p-toluenesulfonyl chloride are used as so-called photoacids, which split off protons during UV irradiation.
• Note that R could be a methanesulfonyl CH 2 O 2 S ( Ms ), or a toluenesulfonyl CH 3 C 6 H 4 O 2 S ( Ts ).
• Other types of ester are prepared in a similar manner for example, tosyl ( tosylate ) esters are made by reaction of the alcohol with p-toluenesulfonyl chloride in pyridine.
• "' 4-Toluenesulfonyl chloride "'( p-toluenesulfonyl chloride, toluene-p-sulfonyl chloride ) is an organic compound with the formula CH 3 C 6 H 4 SO 2 Cl.
• "' 4-Toluenesulfonyl chloride "'( p-toluenesulfonyl chloride, toluene-p-sulfonyl chloride ) is an organic compound with the formula CH 3 C 6 H 4 SO 2 Cl.
• This group is usually derived from the compound para orientation illustrated ( " p "-toluenesulfonyl ) is most common, and by convention " tosyl " refers to the " p "-toluenesulfonyl group.
• This group is usually derived from the compound para orientation illustrated ( " p "-toluenesulfonyl ) is most common, and by convention " tosyl " refers to the " p "-toluenesulfonyl group.