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Atomfair Prolinol C5H11NO

Description Prolinol (Pyrrolidin-2-ylmethanol) is a high-purity chiral compound with the molecular formula C5H11NO (CAS No. 68832-13-3). This versatile heterocyclic alcohol features a pyrrolidine ring with a hydroxymethyl substituent, making it a valuable building block in asymmetric synthesis and pharmaceutical research. Available in >98% purity by GC, our Prolinol is rigorously tested for identity, potency, and impurities to meet the stringent requirements of research and industrial applications. The compound is supplied in amber glass bottles under inert atmosphere to ensure stability, with options for bulk quantities. Ideal for use as a ligand in metal-catalyzed reactions, a precursor for chiral auxiliaries, or…

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Description

Description

Prolinol (Pyrrolidin-2-ylmethanol) is a high-purity chiral compound with the molecular formula C5H11NO (CAS No. 68832-13-3). This versatile heterocyclic alcohol features a pyrrolidine ring with a hydroxymethyl substituent, making it a valuable building block in asymmetric synthesis and pharmaceutical research. Available in >98% purity by GC, our Prolinol is rigorously tested for identity, potency, and impurities to meet the stringent requirements of research and industrial applications. The compound is supplied in amber glass bottles under inert atmosphere to ensure stability, with options for bulk quantities. Ideal for use as a ligand in metal-catalyzed reactions, a precursor for chiral auxiliaries, or a scaffold in medicinal chemistry.

  • CAS No: 68832-13-3
  • Molecular Formula: C5H11NO
  • Molecular Weight: 101.15
  • Exact Mass: 101.084063974
  • Monoisotopic Mass: 101.084063974
  • IUPAC Name: pyrrolidin-2-ylmethanol
  • SMILES: C1CC(NC1)CO
  • Synonyms: pyrrolidin-2-ylmethanol, 498-63-5, Prolinol, (pyrrolidin-2-yl)methanol, pyrrolidine-2-methanol

Application

Prolinol serves as a key chiral intermediate in the synthesis of pharmaceuticals and agrochemicals. Its pyrrolidine structure makes it valuable for constructing bioactive molecules with stereochemical control. The compound is widely used as a ligand in asymmetric catalysis, particularly in enantioselective C-C bond forming reactions. Researchers also employ Prolinol derivatives as organocatalysts in aldol and Michael addition reactions.

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