Product Data Sheet

Hept-6-yn-1-yl 4-methylbenzenesulfonate

Catalog No. A89431

main product photo
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.
Chemical Information
Catalog NumA89431
M. Wt266.36
FormulaC14H18O3S
Purity>98%
Storageat -20 °C 3 years (powder form); at -20 °C 6 months (Solution base)
CAS No.87462-63-3
Synonyms
SMILESC#CCCCCCOS(C1=CC=C(C)C=C1)(=O)=O
Biological Activity
DescriptionHept-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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