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Structure of 170848-34-7
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This chiral building block features a protected amino group and a reactive iodopropionic ester moiety, enabling selective conjugation in peptide synthesis. The tert-butyl carbamate handle ensures stability during purification, while the methyl ester facilitates downstream transformations.
(S)-2-[(tert-Butoxycarbonyl)amino]-3-iodopropionic acid methyl ester serves as a versatile chiral building block for the synthesis of β-amino acids and peptidomimetics. The iodide functionality enables palladium-catalyzed cross-coupling reactions, while the Boc-protected amine and ester groups offer orthogonal handling and compatibility with standard peptide synthesis workflows. Bench-stable and readily purified by flash chromatography, it facilitates efficient access to biologically relevant scaffolds.
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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: