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CAS RN: 1155843-79-0 | Product Number: H1404
2-Hydroxy-2-azaadamantane
Purity: >98.0%(T)
Synonyms:
- AZADOL®
Product Documents:
Size | Unit Price | Same Day | 2-3 Business Days |
---|---|---|---|
200MG |
$44.00
|
4 | Contact Us |
1G |
$134.00
|
6 | 11 |
5G |
$461.00
|
11 | 6 |
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TCI
to order our products. The above prices do not include freight cost, customs, and other charges to the destination.
* The storage conditions are subject to change without notice.
Supplemental Product Information:
AZADOL® is a registered trademark of Nissan Chemical Industries, Ltd.
Product Number | H1404 |
Purity / Analysis Method | >98.0%(T) |
Molecular Formula / Molecular Weight | C__9H__1__5NO = 153.23 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
Packaging and Container | 1G-Glass Bottle with Plastic Insert (View image), 200MG-Glass Bottle with Plastic Insert (View image) |
CAS RN | 1155843-79-0 |
Reaxys Registry Number | 21286916 |
PubChem Substance ID | 172089100 |
Specifications
Appearance | White to Gray to Brown powder to crystal |
Purity(GC) | min. 97.0 % |
Purity(Nonaqueous Titration) | min. 98.0 % |
NMR | confirm to structure |
Properties (reference)
GHS
Related Laws:
Transport Information:
H.S.code* | 2933.99-000 |
Application
AZADO Catalyzed One-Pot Oxidative Cleavage of Vicinal Diols to (Di)Carboxylic Acids
Typical Procedure (R1 = BzO(CH2)7-, R2 = H): To a solution of 9,10-dihydroxydecyl benzoate (30.0 mg, 0.102 mmol) in CH2Cl2 (0.26 mL) and H2O (0.26 mL) is added AZADOL (1.6 mg, 0.0102 mmol) and PhI(OAc)2 (164 mg, 0.510 mmol) at 0 °C. The mixture is allowed to warm to room temperature and stirred for 1 h. Then, 10% HCl is added to the mixture and the resultant solution is extracted with CH2Cl2. The combined organic layer is washed with brine, dried over MgSO4 and concentrated under reduced pressure. The crude product is purified by silica gel column chromatography (eluent: AcOEt/Hexane = 1/8 to only AcOEt) to give 9-(benzoyloxy)nonanoic acid (26.8 mg, 0.0963 mmol, 94%) as white solid.
References
- 1)M. Shibuya, T. Shibuta, H. Fukuda, Y. Iwabuchi, Org. Lett. 2012, 14, 5010.
- 2)A review on AZADO for oxidation of alcohols.
Application
Alcohol Oxidation Catalyst Showing Higher Activity than TEMPO
References
- 1)Y. Iwabuchi, Chem. Pharm. Bull. 2013, 61, 1197.
- 2)M. Shibuya, Y. Sasano, M. Tomizawa, T. Hamada, M. Kozawa, N. Nagahama, Y. Iwabuchi, Synthesis 2011, 3418.
- 3)Y. Iwabuchi, M. Shibuya, M. Tomizawa, Y. Osada, PCT Int. Appl. WO 2009145323, 2009.
- 4)M. Hayashi, M. Shibuya, Y. Iwabuchi, Org. Lett. 2012, 14, 154.
PubMed Literature
Articles/Brochures
TCIMAIL
[Product Highlights] Alcohol Oxidation Catalyst Showing Higher Activity than TEMPO[Research Articles] AZADO Catalyzed One-Pot Oxidative Cleavage of Vicinal Diols to (Di)Carboxylic Acids
Product Documents (Note: Some products will not have analytical charts available.)
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