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Structure of 190906-92-4
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tert-Butyl 2-methyl-4-oxopiperidine-1-carboxylate features a sterically hindered piperidine core with a ketone at the C4 position, enabling selective functionalization. The tert-butyl ester group provides stability and convenient deprotection under mild acidic conditions, making this scaffold valuable for building complex nitrogen-containing architectures in medicinal chemistry and natural product synthesis.
tert-Butyl 2-methyl-4-oxopiperidine-1-carboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted piperidines via reductive amination or nucleophilic addition at the C4 carbonyl. The tert-butyl carbamate group provides excellent stability and convenient removal under mild acidic conditions. Its bench-stable nature, functional group tolerance, and compatibility with standard coupling and reduction protocols make it ideal 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: