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Atomfair (S)-Bis(4-methoxyphenyl)(pyrrolidin-2-yl)methanol C19H23NO3

Description (S)-Bis(4-methoxyphenyl)(pyrrolidin-2-yl)methanol (CAS No. 131180-57-9) is a high-purity chiral compound with the molecular formula C19H23NO3. This optically active pyrrolidine derivative features a central methanolic group flanked by two 4-methoxyphenyl substituents, making it a valuable intermediate in asymmetric synthesis and pharmaceutical research. The compound’s stereochemistry (S-configuration) is particularly useful for enantioselective transformations. Supplied as a white to off-white crystalline solid with ??95% purity (HPLC), it is ideal for catalysis development, ligand design, and medicinal chemistry applications. Store under inert atmosphere at 2-8??C to maintain stability.

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Description

Description

(S)-Bis(4-methoxyphenyl)(pyrrolidin-2-yl)methanol (CAS No. 131180-57-9) is a high-purity chiral compound with the molecular formula C19H23NO3. This optically active pyrrolidine derivative features a central methanolic group flanked by two 4-methoxyphenyl substituents, making it a valuable intermediate in asymmetric synthesis and pharmaceutical research. The compound’s stereochemistry (S-configuration) is particularly useful for enantioselective transformations. Supplied as a white to off-white crystalline solid with ??95% purity (HPLC), it is ideal for catalysis development, ligand design, and medicinal chemistry applications. Store under inert atmosphere at 2-8??C to maintain stability.

  • CAS No: 131180-57-9
  • Molecular Formula: C19H23NO3
  • Molecular Weight: 313.4
  • Exact Mass: 313.16779360
  • Monoisotopic Mass: 313.16779360
  • IUPAC Name: bis(4-methoxyphenyl)-pyrrolidin-2-ylmethanol
  • SMILES: COC1=CC=C(C=C1)C(C2CCCN2)(C3=CC=C(C=C3)OC)O
  • Synonyms: (S)-Bis(4-methoxyphenyl)(pyrrolidin-2-yl)methanol, SCHEMBL2043678, GFA18057

Application

This compound serves as a key chiral building block for asymmetric catalysis in pharmaceutical synthesis. Researchers utilize it to develop novel ligands for transition metal-catalyzed reactions. The methoxy-substituted aromatic rings enhance electron density, making it useful for studying structure-activity relationships in drug discovery.

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