58173-92-5

Basic information

• Product Name: Cyclohexanone, 2-(methoxymethyl)-
• Synonyms: 2-Methoxymethyl-cyclohexanon
• CAS NO: 58173-92-5
• Molecular Formula: C8H14O2
• Molecular Weight: 142.198
• Mol File: 58173-92-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Cyclohexanone, 2-(methoxymethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanone, 2-(methoxymethyl)-(58173-92-5)
• EPA Substance Registry System: Cyclohexanone, 2-(methoxymethyl)-(58173-92-5)

Safety Data

• Hazardous Substances Data: 58173-92-5(Hazardous Substances Data)

Upstream product

• 1125-99-1 1-(1-Cyclohexen-1-yl)pyrrolidine 
• 107-30-2 chloromethyl methyl ether 
• 1424-22-2 1-cyclohexenyl acetate 
• 109-87-5 Dimethoxymethane 
• 6651-36-1 1-(Trimethylsilyloxy)cyclohexene 
• 5331-08-8 2-(hydroxymethyl)cyclohexanone 
• 74-88-4 methyl iodide 
• 1059-49-0 2,2-Bis-tosyloxymethyl-cyclohexan-1-on 

Downstream Products

• 92862-96-9 (2-(methoxymethyl)cyclohex-1-enyl)benzene 
• 97118-36-0 2-Methoxymethyl-1-phenyl-cyclohexan 
• 96620-54-1 2-Methyl-1-phenyl-4,5-dihydrobenzol 
• 17057-95-3 1,2,3,4-tetrahydro-9H-fluorene 

Relevant articles and documents

Carbon-carbon bond forming reactions by using bistrifluoromethanesulfonimide

Bistrifluoromethanesulfonimide has been used to catalyze C-C bond forming reactions such as Friedel-Crafts, Mukaiyama, 1,2-addition and 1,4-addition as well as C-glycosidation reactions.

TRIMETHYLSILYL TRIFLATE CATALYZED ALDOL-TYPE REACTION OF ENOL SILYL ETHERS AND ACETALS OR RELATED COMPOUNDS

Trimethylsilyl triflate with or without added hindered tertiary amines catalyzes directed condensation of enol trimethylsilyl ethers with acetals, orthoformate, or 2-acetoxytetrahydrofuran or -pyrans to give the corresponding β-alkoxy carbonyl compounds.R

CONDENSATION OF ENOL SILYL ETHERS AND DIALKOXYMETHANES CATALYZED BY TRIMETHYLSILYL TRIFLUOROMETHANESULFONATE. REGIOSPECIFIC SYNTHESIS OF α-ALKOXYMETHYL KETONES

A facile, regiospecific entry to α-alkoxymethyl ketones is described.