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Structure of 158690-56-3
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This sulfonate ester features a tert-butoxycarbonyl-protected amine tethered to a 4-methylbenzenesulfonate leaving group. It enables selective amidation reactions under mild conditions, leveraging the stability of the Boc moiety and the reactivity of the aryl sulfonate. Ideal for peptide synthesis and bioconjugation workflows requiring orthogonal functionalization.
2-((tert-Butoxycarbonyl)amino)ethyl 4-methylbenzenesulfonate serves as a versatile, bench-stable sulfonate ester for the introduction of protected amine functionalities in synthetic sequences. It facilitates efficient nucleophilic substitution reactions with diverse amines, enabling rapid access to N-Boc aminoalkyl derivatives under mild conditions. Its excellent functional group tolerance and straightforward purification profile make it ideal for building blocks in peptide synthesis and medicinal chemistry campaigns.
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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-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: