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Structure of 270263-03-1
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(S)-3-((tert-Butoxycarbonyl)amino)hex-5-enoic acid features a chiral center and a terminal alkene, enabling selective conjugate additions and downstream transformations. The Boc-protected amine ensures stability during storage and handling, while the enoic acid moiety facilitates Michael addition reactions in peptide and natural product synthesis.
(S)-3-((tert-Butoxycarbonyl)amino)hex-5-enoic acid serves as a versatile chiral building block for the synthesis of bioactive peptides and heterocyclic scaffolds. The protected amine and terminal alkene enable selective functionalization, while the tert-butyl carbamate group offers stability and convenient removal under mild acidic conditions. Its defined stereochemistry and compatibility with standard coupling reactions make it ideal for iterative peptide assembly and late-stage diversification 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-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: