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Structure of 52574-06-8
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(S)-1-Methyl-5-oxopyrrolidine-2-carboxylic acid features a chiral pyrrolidine core with a methylated nitrogen and a ketone-functionalized ring, enabling precise stereochemical control in peptide bond mimicry. This stable, bench-ready scaffold integrates readily into bioactive molecules, offering enhanced metabolic resilience and favorable conformational rigidity for medicinal chemistry applications.
(S)-1-Methyl-5-oxopyrrolidine-2-carboxylic acid serves as a versatile chiral building block in medicinal chemistry, enabling the synthesis of pyrrolidinone-containing scaffolds prevalent in bioactive molecules. Its well-defined stereochemistry and stability under standard reaction conditions facilitate efficient incorporation into peptide-like frameworks and heterocyclic systems. Functions as a key intermediate in the construction of kinase inhibitors and CNS-targeted compounds, offering predictable reactivity in amide coupling and reduction processes.
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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: