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Structure of 1192373-48-0
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tert-Butyl hept-6-yn-1-ylcarbamate features a terminal alkyne group flanked by a robust tert-butyl carbamate protecting group, enabling stable storage and selective deprotection. This bifunctional scaffold integrates seamlessly into copper-catalyzed click chemistry workflows and supports efficient conjugation in peptide synthesis and bioconjugation applications.
tert-Butyl hept-6-yn-1-ylcarbamate serves as a versatile, bench-stable building block for the synthesis of alkyne-containing scaffolds. Its terminal alkyne functionality enables efficient copper-catalyzed azide-alkyne cycloaddition (CuAAC), while the tert-butoxycarbonyl (Boc) group provides orthogonal protection for primary amines. The molecule exhibits excellent functional group tolerance and facilitates straightforward purification, making it well-suited for iterative peptide and heterocyclic compound assembly in medicinal chemistry workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P501
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Lot numbers can be found on the outside label of a product: