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Structure of 741737-30-4
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tert-Butyl 2-methyl-3-oxopiperidine-1-carboxylate features a sterically hindered piperidine core with a ketone at C3 and a bench-stable tert-butyloxycarbonyl group. This scaffold integrates readily into complex molecular architectures, enabling efficient access to bioactive nitrogen-containing frameworks through selective reduction and subsequent functionalization.
tert-Butyl 2-methyl-3-oxopiperidine-1-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient access to piperidine-based scaffolds. The ketone functionality at C3 supports selective reduction, enolate formation, and nucleophilic addition, while the tert-butyl carbamate group provides stability and convenient deprotection under mild acidic conditions. Its compatibility with standard coupling and functionalization protocols makes it ideal for iterative synthesis of complex heterocycles and API 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: