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Structure of 2091951-57-2
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tert-Butyl (R)-3-methyl-4-oxopiperidine-1-carboxylate features a chiral piperidine core with a stereodefined methyl group and a ketone at the 4-position, enabling selective functionalization in asymmetric synthesis. The tert-butyl carbamate handle ensures stability and ease of removal under mild acidic conditions. This scaffold serves as a key building block for bioactive alkaloids and pharmaceutical intermediates.
tert-Butyl (R)-3-methyl-4-oxopiperidine-1-carboxylate serves as a versatile chiral building block for the synthesis of piperidine-based pharmaceuticals and bioactive molecules. The protected amine and ketone functionalities enable sequential functionalization, including reductive amination and nucleophilic addition, with excellent stereocontrol. Its bench-stable nature and compatibility with standard coupling reactions facilitate efficient route development in medicinal chemistry.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: