72009-05-3

Basic information

• Product Name: 2-Methyl-6-(2-oxopropyl)cyclohexanone
• CAS NO: 72009-05-3
• Molecular Weight: 168.236
• Mol File: 72009-05-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-Methyl-6-(2-oxopropyl)cyclohexanone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Methyl-6-(2-oxopropyl)cyclohexanone(72009-05-3)
• EPA Substance Registry System: 2-Methyl-6-(2-oxopropyl)cyclohexanone(72009-05-3)

Safety Data

• Hazardous Substances Data: 72009-05-3(Hazardous Substances Data)

Upstream product

• 5049-51-4 6-methyl-1-pyrrolidino-1-cyclohexene 
• 4749-28-4 2-nitropropene 
• 193468-09-6 [2-Methyl-cyclohex-(E)-ylidene]-((S)-1-phenyl-ethyl)-amine 
• 105104-40-3 Okahara's reagent 
• 583-60-8 2-Methylcyclohexanone 
• 72009-03-1 2-methyl-2-(2-chloro-2-propenyl)cyclohexanone 
• 5758-08-7 anti-2a-Methyl-cyclohexanon-N,N-dimethylhydrazon 
• 76634-95-2 3-chloro-2-(trimethylsilyloxy)prop-1-ene 
• 20007-02-7 cyclohexyl(2-methylcyclohexylidene)amine 
• 20007-02-7 N-(2-methylcyclohexylidene)cyclohexylamine 
• 73336-26-2 2-(2-Bromallyl)-6-methylcyclohexanon 
• 19980-33-7 6-methyl-1-trimethylsiloxycyclohex-1-ene 

Relevant articles and documents

Nitroalkenes as electrophiles in the asymmetric Michael reaction involving chiral imines/enamino esters

Addition of 2-nitropropene to the chiral imine derived from 2- methylcyclopentanone and (S)-1-phenylethylamine furnished the expected Michael adduct. The latter compound was then efficiently converted into (R)- pentalenone through a Nef reaction. Condensa

1,4- and 1,5-Diketones via Palladium-Catalyzed Allylation of Potassium Enoxyborates

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3-Chloro-2-(trimethylsiloxy)-1-propene as an Electrophilic Acetonyl Equivalent. A Novel Regioselective Synthesis of 1,4-Dicarbonyl Compounds

α-Metalated imines, hydrazones, and activated methylene compounds are acetonylated with 3-chloro-2-(trimethylsiloxy)-1-propene in high yield.Highly regioselective acetonylation at either the tertiary or secondary α-carbon of 2-methylcyclohexanone can be carried out by selecting the reaction conditions.