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Atomfair (2R,3S)-3-hydroxyproline amide C5H10N2O2

Description (2R,3S)-3-hydroxyproline amide (CAS No. 1272669-30-3) is a high-purity chiral compound with the molecular formula C5H10N2O2and IUPAC name (2R,3S)-3-hydroxypyrrolidine-2-carboxamide . This specialized proline derivative is synthesized under stringent conditions to ensure optimal enantiomeric purity, making it an essential building block for peptide synthesis, medicinal chemistry, and asymmetric catalysis. With its hydroxyl and carboxamide functional groups, it serves as a versatile intermediate for drug discovery and biochemical research. Available in research quantities with comprehensive analytical data (HPLC, NMR, MS), this compound is ideal for pharmaceutical development and academic studies. Store in a cool, dry environment to maintain stability.

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Description

Description

(2R,3S)-3-hydroxyproline amide (CAS No. 1272669-30-3) is a high-purity chiral compound with the molecular formula C5H10N2O2 and IUPAC name (2R,3S)-3-hydroxypyrrolidine-2-carboxamide. This specialized proline derivative is synthesized under stringent conditions to ensure optimal enantiomeric purity, making it an essential building block for peptide synthesis, medicinal chemistry, and asymmetric catalysis. With its hydroxyl and carboxamide functional groups, it serves as a versatile intermediate for drug discovery and biochemical research. Available in research quantities with comprehensive analytical data (HPLC, NMR, MS), this compound is ideal for pharmaceutical development and academic studies. Store in a cool, dry environment to maintain stability.

  • CAS No: 1272669-30-3
  • Molecular Formula: C5H10N2O2
  • Molecular Weight: 130.15
  • Exact Mass: 130.074227566
  • Monoisotopic Mass: 130.074227566
  • IUPAC Name: (2R,3S)-3-hydroxypyrrolidine-2-carboxamide
  • SMILES: C1CN[C@H]([C@H]1O)C(=O)N
  • Synonyms: SCHEMBL1442992, (2R,3S)-3-hydroxyproline amide, HTJXCQYXFPTUOW-IUYQGCFVSA-N, AKOS006346917

Application

(2R,3S)-3-hydroxyproline amide is widely used as a chiral scaffold in the synthesis of bioactive peptides and peptidomimetics. Its stereochemistry makes it valuable for designing enzyme inhibitors and receptor modulators in drug discovery. Researchers also employ it as a ligand in asymmetric catalysis to achieve high enantioselectivity in organic transformations.

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