2,6-Dichloropyridine N-oxide (CAS 2587-00-0)
QUICK LINKS
2,6-Dichloropyridine N-oxide is a chemical compound that functions as a potent oxidizing agent in various chemical reactions. Its mechanism of action involves the transfer of oxygen atoms to other molecules, leading to the oxidation of these substrates. 2,6-Dichloropyridine N-Oxide is known to participate in redox reactions, where it acts as an electron acceptor, facilitating the conversion of organic compounds to their corresponding oxides. In experimental applications, 2,6-Dichloropyridine N-oxide is utilized to induce specific chemical transformations by promoting the oxidation of target molecules. Its mechanism of action involves the formation of reactive oxygen species, which can initiate a cascade of chemical reactions leading to the desired products. 2,6-Dichloropyridine N-Oxide′s functional role lies in its ability to drive oxidation reactions, making it useful for seeking to modify organic molecules in a controlled manner.
2,6-Dichloropyridine N-oxide (CAS 2587-00-0) References
- Asymmetric epoxidation with a photoactivated [Ru(salen)] complex. | Nakata, K., et al. 2001. Chemistry. 7: 3776-82. PMID: 11575779
- Soluble polymer-supported ruthenium porphyrin catalysts for epoxidation, cyclopropanation, and aziridination of alkenes. | Zhang, JL. and Che, CM. 2002. Org Lett. 4: 1911-4. PMID: 12027645
- Chiral ruthenium porphyrin encapsulated in ordered mesoporous molecular sieves (MCM-41 and MCM-48) as catalysts for asymmetric alkene epoxidation and cyclopropanation. | Zhang, JL., et al. 2002. Chem Commun (Camb). 2906-7. PMID: 12478806
- The remote-oxyfunctionalization of unactivated carbons in (5 beta)-3-oxobile acids by 2,6-dichloropyridine N-oxide catalyzed by ruthenium-porphyrin and HBr: a direct lactonization at C-20. | Ogawa, S., et al. 2004. Org Biomol Chem. 2: 1013-8. PMID: 15034624
- Photoassisted oxygenation of alkane catalyzed by ruthenium complexes using 2,6-dichloropyridine N-oxide under visible light irradiation. | Yamaguchi, M., et al. 2004. Chem Commun (Camb). 798-9. PMID: 15045069
- Biomimetic oxidation of unactivated carbons in steroids by a model of cytochrome P-450, oxorutheniumporphyrinate complex. | Lida, T., et al. 2004. Lipids. 39: 873-80. PMID: 15669763
- Dichlororuthenium(IV) complex of meso-tetrakis(2,6-dichlorophenyl)porphyrin: active and robust catalyst for highly selective oxidation of arenes, unsaturated steroids, and electron-deficient alkenes by using 2,6-dichloropyridine N-oxide. | Zhang, JL. and Che, CM. 2005. Chemistry. 11: 3899-914. PMID: 15812875
- Site-isolated porphyrin catalysts in imprinted polymers. | Burri, E., et al. 2005. Chemistry. 11: 5055-61. PMID: 15977282
- Fast catalytic hydroxylation of hydrocarbons with ruthenium porphyrins. | Wang, C., et al. 2006. Inorg Chem. 45: 4769-82. PMID: 16749842
- Enantiotopos-selective C-H oxygenation catalyzed by a supramolecular ruthenium complex. | Frost, JR., et al. 2015. Angew Chem Int Ed Engl. 54: 691-5. PMID: 25413591
- Displacement of Dinitrogen by Oxygen: A Methodology for the Catalytic Conversion of Diazocarbonyl Compounds to Ketocarbonyl Compounds by 2,6-Dichloropyridine-N-oxide. | Yu, Y., et al. 2018. Org Lett. 20: 776-779. PMID: 29345129
- Gold(I)-Catalyzed Oxidation of Acyl Acetylenes to Vicinal Tricarbonyls. | Dubovtsev, AY., et al. 2019. Org Lett. 21: 4116-4119. PMID: 31090426
- Gold catalyzed efficient preparation of dihydrobenzofuran from 1,3-enyne and phenol. | Wang, YJ., et al. 2021. Chem Commun (Camb). 57: 12607-12610. PMID: 34755721
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2,6-Dichloropyridine N-oxide, 1 g | sc-231177 | 1 g | $22.00 |