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Structure of 16217-15-5
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(S)-1-Benzyl 2-methyl 4-oxopyrrolidine-1,2-dicarboxylate features a chiral pyrrolidine core with orthogonal functional handles: a benzyl ester and a methyl-substituted carbonyl. This configuration enables selective derivatization in asymmetric synthesis, particularly for peptidomimetics and nitrogen-containing heterocycles. The compound exhibits bench-stable handling characteristics and compatibility with standard amine coupling protocols.
(S)-1-Benzyl 2-methyl 4-oxopyrrolidine-1,2-dicarboxylate serves as a versatile chiral building block in asymmetric synthesis, enabling efficient access to pyrrolidine-based scaffolds. Its defined stereochemistry and orthogonal functional groups facilitate selective transformations, including reductive amination and nucleophilic substitution, while its bench-stable nature supports straightforward handling and purification in 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-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: