89616-30-8

Basic information

• Product Name: 2-chloro-5-methyl-cyclohexanone
• CAS NO: 89616-30-8
• Molecular Weight: 146.617
• Mol File: 89616-30-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-chloro-5-methyl-cyclohexanone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-chloro-5-methyl-cyclohexanone(89616-30-8)
• EPA Substance Registry System: 2-chloro-5-methyl-cyclohexanone(89616-30-8)

Safety Data

• Hazardous Substances Data: 89616-30-8(Hazardous Substances Data)

Upstream product

• 56-23-5 tetrachloromethane 
• 7791-25-5 sulfuryl dichloride 
• 13368-65-5 (3R)-3-methylcyclohexanone 
• 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 
• 793687-71-5 2-chloro-5-methyl-cyclohexanol 

Downstream Products

• 1347703-61-0 2-chloro-5-methylcyclohexanone O-(tert-butyldimethylsilyl)oxime 
• 6240-43-3 cis-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 
• 24070-68-6 3-methylcyclopentanecarboxylic acid 
• 932-51-4 2,5-dimethylcyclohexanone 
• 24070-69-7 1-(3-methylcyclopentyl)ethanone 
• 7214-50-8 5-methylcyclohex-2-en-1-one 

Relevant articles and documents

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.

2,2'-Azoimidazoles as potential cytostatic agents. 9. Condensations with hydrazin-N,N'-dicarbonic acid diamidine

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