C7H7N3O2S is reagent was prepared by in situ reaction of p-toluenesulfonyl chloride with sodium azide before use. The reaction conditions were simple and mild.
osyl azide is used for the introduction of azide and diazo functional groups.[1] It is also used as a nitrene source and as a substrate for cycloaddition reactions. Tosyl azide can be prepared by the reaction of tosyl chloride with sodium azide in aqueous acetone.
Tosyl Azide is one of the more stable azide compounds but is still regarded as a potential explosive and should be carefully stored.Pharmaceutical Intermediates suppliers
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18th July 2018
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