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Structure of 26566-11-0
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(R)-4-(((Benzyloxy)carbonyl)amino)-5-methoxy-5-oxopentanoic acid features a chiral center at the C4 position, enabling stereocontrolled synthesis in peptide and macrocycle workflows. The benzyloxycarbonyl (Cbz) group provides robust N-terminal protection, while the methoxy-ketone functionality offers a handle for selective derivatization under mild conditions. This compound combines stability with orthogonal reactivity, streamlining access to complex scaffolds.
(R)-4-(((Benzyloxy)carbonyl)amino)-5-methoxy-5-oxopentanoic acid serves as a versatile building block for the synthesis of β-amino carbonyl compounds and heterocyclic scaffolds. Its well-defined stereochemistry and orthogonal functionality—combining a benzyl ester, amine, and α-ketoester group—enable selective transformations in peptide-like sequences and complex molecule assembly. Bench-stable and amenable to standard purification methods, it facilitates efficient downstream derivatization in medicinal chemistry and process development 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: