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Atomfair 9-Azabicyclo[3.3.1]nonanen-oxyl C8H14NO
Description 9-Azabicyclo[3.3.1]nonanen-oxyl (CAS No. 31785-68-9) is a highly specialized bicyclic nitroxyl radical compound with the molecular formula C8H14NO . This stable free radical is widely utilized in organic synthesis, catalysis, and as a spin label in biophysical studies due to its unique structural and electronic properties. The rigid bicyclic framework enhances stability, making it ideal for applications requiring persistent radical behavior. Available in high purity (>98%), this compound is supplied as a crystalline solid or solution, with rigorous QC testing to ensure batch-to-batch consistency. Store under inert conditions at -20??C to prevent degradation. Synonyms include AKOS028109619 and AKOS037621291 .
Description
Description
9-Azabicyclo[3.3.1]nonanen-oxyl (CAS No. 31785-68-9) is a highly specialized bicyclic nitroxyl radical compound with the molecular formula C8H14NO. This stable free radical is widely utilized in organic synthesis, catalysis, and as a spin label in biophysical studies due to its unique structural and electronic properties. The rigid bicyclic framework enhances stability, making it ideal for applications requiring persistent radical behavior. Available in high purity (>98%), this compound is supplied as a crystalline solid or solution, with rigorous QC testing to ensure batch-to-batch consistency. Store under inert conditions at -20??C to prevent degradation. Synonyms include AKOS028109619 and AKOS037621291.
- CAS No: 31785-68-9
- Molecular Formula: C8H14NO
- Molecular Weight: 140.20
- Exact Mass: 140.107539070
- Monoisotopic Mass: 140.107539070
- SMILES: C1CC2CCCC(C1)N2[O]
- Synonyms: 9-azabicyclo[3.3.1]nonanen-oxyl, AKOS028109619, AKOS037621291
Application
9-Azabicyclo[3.3.1]nonanen-oxyl serves as a versatile spin probe in EPR spectroscopy for studying molecular dynamics and membrane interactions. It is also employed as a catalyst in oxidation reactions and as a building block for nitroxide-mediated polymerization (NMP). Researchers leverage its stable radical nature in the development of advanced materials and redox-active systems.
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