118082-04-5

Basic information

• Product Name: 2-butyryl-5,5-dimethyl-3-methoxy-6-methoxycarbonyl-2-cyclohexen-1-one
• Synonyms: 2-butyryl-5,5-dimethyl-3-methoxy-6-methoxycarbonyl-2-cyclohexen-1-one
• CAS NO: 118082-04-5
• Molecular Weight: 282.337
• Mol File: 118082-04-5.mol

Chemical Properties

• CAS DataBase Reference: 2-butyryl-5,5-dimethyl-3-methoxy-6-methoxycarbonyl-2-cyclohexen-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-butyryl-5,5-dimethyl-3-methoxy-6-methoxycarbonyl-2-cyclohexen-1-one(118082-04-5)
• EPA Substance Registry System: 2-butyryl-5,5-dimethyl-3-methoxy-6-methoxycarbonyl-2-cyclohexen-1-one(118082-04-5)

Safety Data

• Hazardous Substances Data: 118082-04-5(Hazardous Substances Data)

Upstream product

• 66421-41-8 2-butyryl-4-methoxycarbonyl-5,5-dimethylcyclohexane-1,3-dione 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 126078-80-6 2-butyryl-5,5-dimethyl-1-methoxy-4-methoxycarbonyl-3-trimethylsilyloxy-1,3-cyclohexadiene 
• 126104-60-7 6-acetoxy-2-butyryl-5,5-dimethyl-3-methoxy-6-methoxycarbonyl-2-cyclohexen-1-one 
• 126279-97-8 2-butyl-5,5-dimethyl-3-methoxy-6-methoxycarbonyl-2-cyclohexen-1-one 
• 126078-78-2 2-butyryl-5,5-dimethyl-3-methoxy-6-methoxycarbonyl-6-chloro-2-cyclohexen-1-one 
• 174842-58-1 3-Butyryl-4-mercapto-6,6-dimethyl-2-oxo-cyclohex-3-enecarboxylic acid methyl ester 
• 174842-60-5 3-Butyryl-4-ethylsulfanyl-6,6-dimethyl-2-oxo-cyclohex-3-enecarboxylic acid methyl ester 
• 126078-79-3 2-butyryl-5,5-dimethyl-4-chloro-1,3-cyclohexanedione 
• 126078-77-1 2-butyryl-4-hydroxy-5,5-dimethyl-1,3-cyclohexanedione 
• 123299-41-2 3-amino-2-butanoyl-6-methoxycarbonyl-5,5-dimethyl-2-cyclohexen-1-one 
• 123299-38-7 2-butanoyl-6-methoxycarbonyl-5,5-dimethyl-3-pyrrolidino-2-cyclohexen-1-one 

Relevant articles and documents

SYNTHESIS OF ENOL METHYL ETHERS OF β-TRIKETONES OF THE CYCLOHEXANE SERIES

During the alkylation of the sodium or tetrabutylammonium salt of 2-butyryl-4-methoxycarbonyl-5,5-dimethylcyclohexane-1,3-dione with dimethyl sulfate in acetone or methylene chloride a mixture of the regioisomeric methyl ethers is formed.The composition of the mixture depends on the reaction conditions.Methyl ethers of other β-triketones in the cyclohexane series were obtained similarly.The structure of the obtained compounds was established by differential spectroscopy of the nuclear Overhauser effect.