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Structure of 15383-56-9
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Sodium (S)-pyrrolidine-2-carboxylate serves as a chiral synthon in asymmetric synthesis, leveraging its well-defined stereochemistry to direct enantioselective transformations. The pyrrolidine ring imparts conformational rigidity, while the carboxylate group enables facile derivatization. This bench-stable salt combines high chemical purity with predictable reactivity, streamlining access to biologically relevant scaffolds in medicinal chemistry and peptide engineering workflows.
Sodium (S)-pyrrolidine-2-carboxylate serves as a chiral building block in asymmetric synthesis, enabling stereoselective transformations through its well-defined C2 chirality and carboxylate functionality. Its bench-stable nature and compatibility with standard peptide coupling protocols facilitate efficient incorporation into complex molecular architectures, including bioactive heterocycles and peptidomimetics.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: