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Structure of 1442483-69-3
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(S)-Methyl 2-((tert-butoxycarbonyl)amino)-3-((S)-2-oxopiperidin-3-yl)propanoate is a chiral dipeptide surrogate featuring a protected α-amino group and a reactive ketone-bearing piperidine ring. This configuration enables direct incorporation into peptide synthesis workflows, where the oxopiperidinyl moiety facilitates cyclization or downstream functionalization under standard conditions. The tert-butyl carbamate group ensures stability during handling and purification.
(S)-Methyl 2-((tert-butoxycarbonyl)amino)-3-((S)-2-oxopiperidin-3-yl)propanoate serves as a key chiral building block for the synthesis of piperidine-containing peptidomimetics and bioactive heterocycles. The protected amino group enables orthogonal deprotection, while the oxopiperidinyl moiety facilitates ring expansion or cyclization reactions. Its bench-stable nature and compatibility with standard coupling protocols make it ideal for modular peptide and medicinal chemistry workflows.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: