89616-30-8

Upstream product

• 591-24-2 3-Methylcyclohexanone 
• 22336-10-3 1-acetoxy-5-methylcyclohexene 
• 7732-18-5 water 
• 7782-50-5 chlorine 
• 70871-31-7 5-Methyl-1-methylsulfanyl-cyclohexene 
• 13368-65-5 (3R)-3-methylcyclohexanone 
• 56-23-5 tetrachloromethane 
• 7791-25-5 sulfuryl dichloride 
• 793687-71-5 2-chloro-5-methyl-cyclohexanol 

Downstream Products

• 24070-68-6 3-methylcyclopentanecarboxylic acid 
• 855383-78-7 optically inactive 1,2-epoxy-1-methoxy-5-methyl-cyclohexane 
• 39511-99-4 2-Hydroxy-5-methyl-1-cyclohexanon 
• 6240-43-3 cis-3-methylcyclopentanecarboxylic acid 
• 1347703-61-0 2-chloro-5-methylcyclohexanone O-(tert-butyldimethylsilyl)oxime 
• 7214-50-8 5-methylcyclohex-2-en-1-one 
• 932-51-4 2,5-dimethylcyclohexanone 
• 24070-69-7 1-(3-methylcyclopentyl)ethanone 

Relevant academic research and scientific papers

Halogenation of carbonyl compounds by an ionic liquid, [AcMIm]X, and Ceric Ammonium Nitrate (CAN)

An ionic liquid, acetylmethylimidazolium halide ([AcMIm]X), in combination with ceric ammonium nitrate promotes halogenations of a wide variety of ketones and 1,3-keto esters at the ?-position. The ionic liquid acts here as reagent as well as reaction medium, and thus the reaction does not require any organic solvent or conventional halogenating agent. The reaction is completely arrested when the radical quencher TEMPO is used. A plausible radical mechanism is also suggested. CSIRO 2007.

Metal-Catalyzed Organic Photoreactions. The Photooxidation of Vinylsilanes and Vinyl Sulfides in the Presence of Iron(III) Chloride, and the Regioselective Synthesis of α-Chloro Ketones

The irradiation of a pyridine solution of vinylsilanes or vinyl sulfides in the presence of iron(III) chloride under oxygen produced α-chloro ketones, with a carbonyl group at the olefinic carbon originally bearing a silicon or sulfur atom.