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Atomfair 3-Oxa-8-azabicyclo[3.2.1]octane C6H11NO

Description 3-Oxa-8-azabicyclo[3.2.1]octane (CAS No. 280-07-9) is a bicyclic organic compound with the molecular formula C6H11NO. This heterocyclic structure features both nitrogen and oxygen atoms within its rigid bicyclo[3.2.1]octane framework, making it a valuable scaffold in medicinal chemistry and pharmaceutical research. The compound is available in high purity (??95%) and is supplied as a clear, colorless to pale yellow liquid under standard conditions. Its unique structural properties lend it to applications in asymmetric synthesis, ligand design, and as a precursor for complex heterocycles. Proper storage at 2-8??C under inert atmosphere is recommended to ensure long-term stability.

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Description

Description

3-Oxa-8-azabicyclo[3.2.1]octane (CAS No. 280-07-9) is a bicyclic organic compound with the molecular formula C6H11NO. This heterocyclic structure features both nitrogen and oxygen atoms within its rigid bicyclo[3.2.1]octane framework, making it a valuable scaffold in medicinal chemistry and pharmaceutical research. The compound is available in high purity (??95%) and is supplied as a clear, colorless to pale yellow liquid under standard conditions. Its unique structural properties lend it to applications in asymmetric synthesis, ligand design, and as a precursor for complex heterocycles. Proper storage at 2-8??C under inert atmosphere is recommended to ensure long-term stability.

  • CAS No: 280-07-9
  • Molecular Formula: C6H11NO
  • Molecular Weight: 113.16
  • Exact Mass: 113.084063974
  • Monoisotopic Mass: 113.084063974
  • IUPAC Name: 3-oxa-8-azabicyclo[3.2.1]octane
  • SMILES: C1CC2COCC1N2
  • Synonyms: 3-oxa-8-azabicyclo[3.2.1]octane, 280-07-9, 3-OXA-8-AZA-BICYCLO[3.2.1]OCTANE, MFCD18250273, (1R,5S)-3-oxa-8-azabicyclo[3.2.1]octane

Application

3-Oxa-8-azabicyclo[3.2.1]octane serves as a key intermediate in the synthesis of pharmacologically active compounds, particularly those targeting neurological receptors. Its constrained bicyclic structure is utilized in developing chiral ligands for asymmetric catalysis. Researchers also employ this heterocycle as a building block for novel drug candidates with potential analgesic or anti-inflammatory properties.

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