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Structure of 161975-39-9
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tert-Butyl 4-(((methylsulfonyl)oxy)methyl)piperidine-1-carboxylate features a piperidine scaffold bearing a methylsulfonyloxy-methyl group, enabling efficient O-alkylation reactions. This bench-stable, moisture-tolerant reagent facilitates selective functionalization in synthetic workflows, particularly in the construction of complex nitrogen-containing architectures.
tert-Butyl 4-(((methylsulfonyl)oxy)methyl)piperidine-1-carboxylate serves as a versatile piperidine-based building block for C–H functionalization and late-stage diversification. The methylsulfonyloxy group enables efficient palladium-catalyzed cross-coupling reactions, while the tert-butyl carbamate protects the amine under standard conditions. Its bench-stable nature and compatibility with diverse reaction partners make it ideal 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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: