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Atomfair 3-Quinuclidinol C7H13NO

Description 3-Quinuclidinol (CAS No. 25333-42-0) is a bicyclic tertiary alcohol with the molecular formula C7H13NO . Its IUPAC name is 1-azabicyclo[2.2.2]octan-3-ol , featuring a rigid quinuclidine scaffold with a hydroxyl group at the 3-position. This heterocyclic compound is a versatile building block in organic synthesis and pharmaceutical research, offering unique stereoelectronic properties due to its bridged structure. Available in high purity grades (??98%), it is supplied as a white crystalline solid with excellent stability under standard storage conditions. Researchers value 3-Quinuclidinol for its role as a precursor to chiral ligands, bioactive molecules, and as a model compound for studying conformational…

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Description

Description

3-Quinuclidinol (CAS No. 25333-42-0) is a bicyclic tertiary alcohol with the molecular formula C7H13NO. Its IUPAC name is 1-azabicyclo[2.2.2]octan-3-ol, featuring a rigid quinuclidine scaffold with a hydroxyl group at the 3-position. This heterocyclic compound is a versatile building block in organic synthesis and pharmaceutical research, offering unique stereoelectronic properties due to its bridged structure. Available in high purity grades (??98%), it is supplied as a white crystalline solid with excellent stability under standard storage conditions. Researchers value 3-Quinuclidinol for its role as a precursor to chiral ligands, bioactive molecules, and as a model compound for studying conformational effects in medicinal chemistry. Suitable for NMR, HPLC, and LC-MS analysis.

  • CAS No: 25333-42-0
  • Molecular Formula: C7H13NO
  • Molecular Weight: 127.18
  • Exact Mass: 127.099714038
  • Monoisotopic Mass: 127.099714038
  • IUPAC Name: 1-azabicyclo[2.2.2]octan-3-ol
  • SMILES: C1CN2CCC1C(C2)O
  • Synonyms: 3-QUINUCLIDINOL, 1619-34-7, Quinuclidin-3-ol, 1-Azabicyclo[2.2.2]octan-3-ol, 3-Hydroxyquinuclidine

Application

3-Quinuclidinol serves as a key intermediate in the synthesis of pharmaceutical compounds, particularly anticholinergic and antispasmodic agents. Its rigid bicyclic structure makes it valuable for developing chiral catalysts and ligands in asymmetric synthesis. The compound is also utilized in neurological research due to its structural similarity to bioactive alkaloids. Additionally, it finds application in material science as a building block for functionalized polymers.

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