Tag OxidizingAgents

Articles by tag "OxidizingAgents"

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  1. Oxidizing Agent-Benzaldehyde Benzaldehyde(C6H5CHO) is an organic compound consisting of a benzene ring with a formyl substituent. It is among the simplest aromatic aldehydes and one of the most industrially useful.
  2. Benzophenone Benzophenone is the organic compound with the formula (C6H5)2CO, generally abbreviated Ph2CO. It is a white solid that is soluble in organic solvents. Benzophenone is a widely used building block in organic chemistry, being the parent diarylketone.
  3. Benzoyl Peroxide (BPO) Benzoyl peroxide is a chemical compound with structural formula (C6H5−C(=O)O−)2, often abbreviated as (BzO)2. In terms of its structure, the molecule can be described as two benzoyl (C6H5−C(=O)−, Bz) groups connected by a peroxide (−O−O−). It is a white granular solid with a faint ...
  4. Sodium Hypochlorite (NaOCl) Sodium hypochlorite is an inexpensive, strong oxidizing agent, that is used as disinfectant and bleaching agent. It is unstable as a solid, but solutions of up to 40% are commercially available that contain NaOH and NaCl as byproducts of the preparation:
  5. N-Bromosaccharin N-Bromosaccharin
  6. N-Bromosuccinimide (NBS) N-Bromosuccinimide (NBS) is a brominating and oxidizing agent that is used as source for bromine in radical reactions (for example: allylic brominations) and various electrophilic additions. The NBS bromination of substrates such as alcohols and amines, followed by elimination of HBr in the ...
  7. Burgess reagent The Burgess reagent, (Methoxycarbonylsulfamoyl)triethylammonium hydroxide is a commercially available compound that has historically found utility as a dehydrating agent. The reagent may also be used to oxidize primary and secondary alcohols to their corresponding aldehydes and ketones in ...
  8. Crotononitrile, (E)-But-2-enenitrile Crotononitrile is a good hydrogen acceptor in ruthenium-catalyzed hydrogen transfer reactions.
  9. N-Fluoro-2,4,6-trimethylpyridinium triflate N-Fluoro-2,4,6-trimethylpyridinium triflate
  10. N-tert-butylbenzenesulfinimidoyl chloride A range of unsymmetrical ketones has been prepared in good yields from aldehydes in one simple synthetic operation by addition of organolithium compounds followed by an oxidation using N-tert-butylphenylsulfinimidoyl chloride.
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