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Structure of 92235-39-7
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(S)-tert-Butyl (2-oxopiperidin-3-yl)carbamate is a chiral building block featuring a protected piperidinone scaffold with defined stereochemistry at the 3-position. This bench-stable, moisture-tolerant reagent integrates seamlessly into peptide synthesis and medicinal chemistry workflows, enabling efficient access to bioactive nitrogen-containing heterocycles through straightforward deprotection and functionalization.
(S)-tert-Butyl (2-oxopiperidin-3-yl)carbamate serves as a key chiral building block in the synthesis of piperidine-containing scaffolds, enabling efficient access to biologically relevant heterocycles. Its stable tert-butyl carbamate group offers excellent protection for primary amines, while the 2-oxo functionality facilitates downstream transformations such as reductive amination and ring expansion. The compound exhibits high bench stability, ease of purification, and compatibility with standard coupling and functionalization protocols, making it well-suited 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: