155200-44-5

Basic information

• Product Name: 2-METHOXYCYCLOHEPTANONE
• Synonyms: 2-METHOXYCYCLOHEPTANONE
• CAS NO: 155200-44-5
• Molecular Formula: C₈H₁₄O₂
• Molecular Weight: 142.197
• Mol File: 155200-44-5.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-METHOXYCYCLOHEPTANONE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-METHOXYCYCLOHEPTANONE(155200-44-5)
• EPA Substance Registry System: 2-METHOXYCYCLOHEPTANONE(155200-44-5)

Safety Data

• Hazardous Substances Data: 155200-44-5(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 18202-04-5 2-Diazacycloheptan-1-one 
• 7429-44-9 2-methoxycyclohexanone 
• 502-42-1 cycloheptanone 
• 50438-50-1 1-methoxycycloheptene 
• 89036-94-2 1-(Benzenesulfonyl-methoxy-methyl)-cyclohexanol 
• 1056246-49-1 2-bromocycloheptanone 

Relevant articles and documents

Reaction of enol ethers with lead tetraacetate : An improved method for the synthesis of α- methoxy ketones

The reaction of cyclic enol ethers with lead tetraacetate in methanol in the presence of BF3.Et2O at 0°C gives α- methoxy cyclic ketones.

Ketone homologation to produce α-methoxyketones: Application to conduritol synthesis

The scope of Trost's sulfone homologation procedure for the conversion of ketones into their α-methoxylated higher homologues has been dramatically expanded. The use of zirconium (or hafnium) tetrachloride in the hydroxy sulfone rearrangement step gives g

ERZEUGUNG UND CYCLOADDITION VON ALLYLIUMIONEN AUS α-HALOGENKETONEN UNTER SOLVOLYSE-BEDINGUNGEN

Some α-haloketones react with furan in methanolic solution in the presence of base to form the 3-oxo-8-oxabicyclooct-6-enes (11), the products derived from a cycloaddition of an allylium intermediate (5 or 6).