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Structure of 129888-60-4
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tert-Butyl 3-((methylsulfonyl)oxy)piperidine-1-carboxylate serves as a stable, bench-ready piperidine scaffold with a latent electrophilic handle. The methylsulfonyloxy group enables efficient displacement reactions under mild conditions, facilitating the introduction of diverse nucleophiles. This reagent integrates seamlessly into synthetic sequences requiring selective functionalization, particularly in medicinal chemistry and process development workflows.
tert-Butyl 3-((methylsulfonyl)oxy)piperidine-1-carboxylate serves as a reliable piperidine-based electrophile for C–H functionalization and late-stage diversification. The methylsulfonyloxy group enables efficient displacement reactions under mild conditions, facilitating the installation of diverse nucleophiles at the C3 position. Its bench-stable nature and compatibility with common protecting groups make it a practical choice for constructing complex heterocyclic scaffolds 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: