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Structure of 119479-32-2
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This protected amino acid derivative features a terminal alkyne functionality flanked by a carboxylic acid and a tert-butoxycarbonyl (Boc)-protected amine. The Boc group ensures stability during synthetic manipulations, while the alkynyl moiety enables efficient coupling via click chemistry. This versatile scaffold integrates readily into peptide-based architectures and bioconjugation workflows under standard conditions.
2-((tert-Butoxycarbonyl)amino)pent-4-enoic acid serves as a versatile building block for the synthesis of bioactive peptides and heterocyclic scaffolds. The conjugated enoic acid moiety enables facile Michael additions and Diels–Alder reactions, while the Boc-protected amine offers orthogonal reactivity and stability under standard synthetic conditions. Its bench-stable nature and ease of purification facilitate efficient incorporation into complex molecular architectures.
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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: