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CS-W001157 4
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Sodium (S)-pyrrolidine-2-carboxylate

  • CAS No. 15383-56-9

  • Cat. No. CS-0091626
  • Purity≥95%
  • MDL No.MFCD23699510

*For research and further manufacturing use only, not for direct human use.

Sodium (S)-pyrrolidine-2-carboxylate|CS-0091626

Structure of 15383-56-9

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General Information

  • CAS No. 15383-56-9
  • Cat. No. CS-0091626
  • Purity ≥95%
  • MDL No. MFCD23699510
  • Storage Store at room temperature, keep dry and cool
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₅H₈NNaO₂
  • Molecular Weight 137.11
  • Synonym(s) L-Proline sodiuM salt
  • SMILES O=C(O[Na])[C@H]1NCCC1

Description

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.

Application

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.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P280-P302+P352

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Computational Chemistry Data

  • TPSA   38.33
  • LogP   -0.6349
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   1

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