Hept-6-yn-1-yl 4-methylbenzenesulfonate functions as a biochemical assay reagent, featuring a tosyl group which serves as an excellent leaving group for nucleophilic substitution reactions. The propargyl moiety enables it to participate in copper-catalyzed azide-alkyne Click Chemistry, facilitating the formation of stable triazole linkages with azide-bearing compounds or biomolecules. This compound is suitable for applications in chemical biology and bioconjugation studies, providing a versatile tool for the synthesis of complex molecular structures.
Hept-6-yn-1-yl 4-methylbenzenesulfonate functions as a biochemical assay reagent, featuring a tosyl group which serves as an excellent leaving group for nucleophilic substitution reactions. The propargyl moiety enables it to participate in copper-catalyzed azide-alkyne Click Chemistry, facilitating the formation of stable triazole linkages with azide-bearing compounds or biomolecules. This compound is suitable for applications in chemical biology and bioconjugation studies, providing a versatile tool for the synthesis of complex molecular structures.
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