9-Azabicyclo[3.3.1]nonane N-oxyl
- Product Name
- 9-Azabicyclo[3.3.1]nonane N-oxyl
- CAS No.
- 31785-68-9
- Chemical Name
- 9-Azabicyclo[3.3.1]nonane N-oxyl
- Synonyms
- ABNO;NPPN;9-azabicyclo[3.3.1]nonan-9-ol;9-Azabicyclo[3.3.1]non-9-yloxy;9-AZABICYCLO[3.3.1]NONANE N-OX;9-Azabicyclo[3.3.1]nonane N-oxyl;9-hydroxy-9-azabicyclo[3.3.1]nonane;9-Azabicyclo[3.3.1]nonane N-oxyl 95%;9-azabiscyclo[3.3.1]nonylalkane-N-oxy;9-Azabicyclo[3.3.1]nonane N-oxyl
- CBNumber
- CB82730770
- Molecular Formula
- C8H14NO*
- Formula Weight
- 140.20286
- MOL File
- 31785-68-9.mol
9-Azabicyclo[3.3.1]nonane N-oxyl Property
- Melting point:
- 65-70°C
- storage temp.
- 2-8°C
- form
- solid
- Appearance
- Brown to reddish brown Solid
- BRN
- 1681761
- InChI
- InChI=1S/C8H14NO/c10-9-7-3-1-4-8(9)6-2-5-7/h7-8H,1-6H2
- InChIKey
- SZAKAAGHPLUEPM-UHFFFAOYSA-N
- SMILES
- C12N([O])C(CCC1)CCC2 |^1:2|
Safety
- Hazard Codes
- Xn
- Risk Statements
- 22-41-52/53
- Safety Statements
- 26-39-61
- WGK Germany
- 3
- Storage Class
- 11 - Combustible Solids
- Hazard Classifications
- Acute Tox. 4 Oral
Eye Dam. 1
N-Bromosuccinimide Price
- Product number
- 763284
- Product name
- 9-Azabicyclo[3.3.1]nonane N-oxyl
- Purity
- 95%
- Packaging
- 50mg
- Price
- $123
- Updated
- 2026/03/19
- Product number
- 763284
- Product name
- 9-Azabicyclo[3.3.1]nonane N-oxyl
- Purity
- 95%
- Packaging
- 1g
- Price
- $456
- Updated
- 2026/03/19
- Product number
- 763284
- Product name
- 9-Azabicyclo[3.3.1]nonane N-oxyl
- Purity
- 95%
- Packaging
- 250mg
- Price
- $264
- Updated
- 2026/03/19
- Product number
- A965460
- Product name
- 9-Azabicyclo[3.3.1]nonane N-oxyl
- Packaging
- 100mg
- Price
- $125
- Updated
- 2021/12/16
- Product number
- FA59534
- Product name
- 9-Azabicyclo[3.3.1]nonane N-oxyl
- Packaging
- 250mg
- Price
- $115
- Updated
- 2021/12/16
9-Azabicyclo[3.3.1]nonane N-oxyl Chemical Properties,Usage,Production
Uses
9-Azabicyclo[3.3.1]nonane N-oxyl (ABNO) may be employed for the aerobic oxidation of alcohols.
General Description
9-Azabicyclo[3.3.1]nonane N-oxyl (ABNO) belongs to a sterically unhindered and stable class of nitroxyl radicals. It efficiently catalyzes the oxidation of alcohols to afford the corresponding carbonyl compounds. ABNO along with (MeObpy)CuI(OTf) (MeObpy =4,4′-dimethoxy-2,2′-bipyridine) comprises a catalytic system. This catalytic system is useful for the aerobic oxidation of all categories of alcohols.
reaction suitability
reagent type: ligand
Synthesis
1. 9-Benzyl-9-azabicyclononan-3-one is reduced to 9-benzyl-9-azabicyclononane in a continuous reactor at 215C with KOH/hydrazine hydrate/ethanol.
2. The product from step 1 is hydrogenated in methanol with Pd/C to remove the benzyl group, yielding 9-azabicyclononane.
3. The product from step 2 is oxidized with urea peroxide catalyzed by sodium tungstate to give the N-oxyl radical.
9-Azabicyclo[3.3.1]nonane N-oxyl Preparation Products And Raw materials
Raw materials
Preparation Products
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