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Structure of 41447-17-0
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(2R)-1-methyl-2-piperidinecarboxylic acid features a chiral piperidine scaffold with a methylated nitrogen and carboxylic acid at the 2-position, enabling precise stereochemical control in peptide-based drug design. This bench-stable derivative integrates readily into peptidomimetic architectures, offering enhanced metabolic stability and improved membrane permeability compared to linear analogs.
(2R)-1-Methyl-2-piperidinecarboxylic acid serves as a valuable chiral building block in medicinal chemistry, enabling the synthesis of bioactive molecules through established amide and ester transformations. Its stereochemical purity supports consistent biological activity in target-directed libraries. The piperidine core provides favorable pharmacokinetic properties, while the carboxylic acid functionality facilitates conjugation via standard coupling reactions. Bench-stable and readily purified by recrystallization, it functions effectively in both small-scale screening 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: