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Structure of 31140-42-8
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tert-Butyl N-(2,6-dioxopiperidin-3-yl)carbamate features a stable carbamate protecting group flanked by two ketone functionalities, enabling selective functionalization in complex molecular scaffolds. This bench-stable reagent integrates readily into peptide and heterocyclic synthesis workflows, offering efficient access to piperidinone derivatives under standard conditions.
tert-Butyl N-(2,6-dioxopiperidin-3-yl)carbamate serves as a versatile synthon in peptide and heterocyclic synthesis, enabling efficient access to piperidine-based scaffolds. Its stability under standard reaction conditions facilitates selective functionalization at the 3-position, while the orthogonal carbamate protection allows for sequential transformations. The molecule functions effectively in amide coupling, nucleophilic displacement, and cyclization reactions, supporting scalable routes to bioactive compounds and pharmaceutical intermediates.
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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: