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Structure of 91028-39-6
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(S)-2-((tert-Butoxycarbonyl)amino)but-3-enoic acid is a chiral building block featuring a vinyl carboxylic acid moiety flanked by a protected amine. This structure enables direct incorporation into peptide backbones and facilitates subsequent deprotection under mild acidic conditions. The tert-butyl carbamate group provides excellent stability during synthetic manipulations, while the electron-rich alkene supports efficient coupling reactions.
(S)-2-((tert-Butoxycarbonyl)amino)but-3-enoic acid serves as a versatile chiral building block for the synthesis of bioactive peptides and heterocyclic scaffolds. The protected amino group enables orthogonal functionalization, while the α,β-unsaturated carboxylic acid moiety facilitates conjugate additions and cycloaddition reactions. Its bench-stable tert-butyl carbamate protection simplifies purification and supports scalable synthesis 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-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: