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Structure of 128781-80-6
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Methyl (S)-2-((tert-butoxycarbonyl)amino)-3-(4-hydroxy-3,5-diiodophenyl)propanoate features a chiral α-amino acid scaffold with a sterically protected Boc group and a highly iodinated phenolic moiety. This bench-stable building block integrates readily into peptide synthesis workflows, enabling efficient access to complex bioactive architectures through orthogonal functionalization.
Methyl (S)-2-((tert-butoxycarbonyl)amino)-3-(4-hydroxy-3,5-diiodophenyl)propanoate serves as a key chiral building block for the synthesis of iodinated aromatic peptides and bioactive heterocycles. The protected amine enables selective coupling reactions, while the diiodophenol moiety facilitates downstream cross-coupling transformations. Bench-stable and readily purified by flash chromatography, it functions as a versatile scaffold in medicinal chemistry campaigns requiring halogenated aromatic systems.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: