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Structure of 218916-64-4
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This protected serine derivative features a tert-butoxycarbonyl group that ensures stability and ease of handling, while the hydroxypropanoic acid moiety provides a reactive site for peptide coupling. Designed for synthetic applications in bioconjugation and peptidomimetic design, it integrates cleanly into complex molecular architectures under standard conditions.
3-((tert-Butoxycarbonyl)amino)-2-hydroxypropanoic acid serves as a stable, bench-ready building block for peptide synthesis and chiral auxiliary development. The protected amino group enables orthogonal functionalization, while the β-hydroxyl moiety supports stereoselective transformations. Its compatibility with standard coupling reagents and ease of purification make it ideal for iterative solid-phase and solution-phase workflows in medicinal chemistry and API intermediate production.
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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: