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Structure of 184368-70-5
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rel-tert-Butyl (2R,6R)-2,6-dimethyl-4-oxopiperidine-1-carboxylate is a stereochemically defined piperidine derivative featuring a bench-stable tert-butyl ester and two methyl groups at the 2- and 6-positions. This configuration enables direct incorporation into asymmetric synthesis workflows, where it serves as a chiral building block for complex heterocycles and bioactive molecule scaffolds.
rel-tert-Butyl (2R,6R)-2,6-dimethyl-4-oxopiperidine-1-carboxylate serves as a stable, bench-ready chiral building block for the synthesis of piperidine-based scaffolds. Its defined stereochemistry and protected carbonyl group enable selective functionalization in late-stage diversification. The tert-butyl ester facilitates straightforward deprotection under mild acidic conditions, while the methyl groups at C2 and C6 enhance conformational rigidity and metabolic stability—key attributes in medicinal chemistry lead optimization.
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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: