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Structure of 1601475-90-4
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(R)-tert-Butyl 3-methyl-5-oxopiperidine-1-carboxylate features a chiral piperidine core with a sterically shielded tert-butyl ester and a ketone at the 5-position. This configuration enables selective functionalization in asymmetric synthesis, particularly for constructing complex nitrogen-containing scaffolds under mild conditions.
(R)-tert-Butyl 3-methyl-5-oxopiperidine-1-carboxylate serves as a versatile chiral building block for the synthesis of bioactive piperidine derivatives. The molecule features a C3-methyl group and a C5 ketone, enabling selective enolate formation and functionalization. Its tert-butyl carbamate protection offers excellent bench stability and facilitates straightforward deprotection under mild acidic conditions. This compound functions effectively in asymmetric synthesis, particularly in constructing substituted piperidines relevant to medicinal chemistry and natural product synthesis.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: