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Structure of 52558-24-4
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This chiral building block features a protected amino group and a hydroxyl-bearing carbon, enabling direct incorporation into peptide syntheses. The tert-butoxycarbonyl (Boc) moiety provides stability under basic conditions, while the hydroxypropanoic acid scaffold offers a handle for derivatization. This configuration supports stereocontrolled assembly of complex bioactive molecules in medicinal chemistry workflows.
(S)-3-((tert-Butoxycarbonyl)amino)-2-hydroxypropanoic acid serves as a stable, bench-ready chiral building block for peptide synthesis and medicinal chemistry. The Boc-protected amine enables orthogonal deprotection in standard workflows, while the β-hydroxy carboxylic acid functionality facilitates stereoselective transformations and incorporation into heterocyclic scaffolds. Its robust stability under ambient conditions and ease of purification make it ideal for multi-step syntheses requiring high reproducibility.
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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: