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Structure of 672883-23-7
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(S)-tert-Butyl (5-oxopyrrolidin-3-yl)carbamate features a chiral pyrrolidinone core with a bench-stable carbamate protecting group, enabling direct incorporation into peptide synthesis workflows. This configuration supports stereoselective transformations and facilitates purification through standard chromatographic methods.
(S)-tert-Butyl (5-oxopyrrolidin-3-yl)carbamate serves as a versatile chiral building block in synthetic organic chemistry, enabling efficient access to pyrrolidine-based scaffolds. Its protected amine functionality offers excellent bench stability and compatibility with diverse reaction conditions, facilitating straightforward deprotection and functionalization. The molecule's inherent stereochemistry supports enantioselective synthesis, while the ketone moiety provides a handle for selective transformations such as reductive amination or nucleophilic addition—making it a practical choice for 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-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: