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Structure of 164323-85-7
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(R)-methyl piperidine-3-carboxylate is a stereochemically defined building block featuring a chiral piperidine core and ester functionality. This bench-stable, moisture-tolerant reagent integrates readily into asymmetric synthesis workflows, enabling direct access to complex nitrogen-containing architectures through selective derivatization at the carboxylate and amine sites.
(R)-Methyl piperidine-3-carboxylate serves as a valuable chiral building block in medicinal chemistry, enabling stereoselective synthesis of bioactive molecules. Its stability under standard reaction conditions and compatibility with diverse functional groups facilitate efficient transformations in peptide-like scaffolds and heterocyclic systems. The molecule functions effectively in coupling reactions, alkylation protocols, and as a precursor to piperidine-based pharmacophores.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 2735
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: