Epoxy cyclohexyl ether

Cyclohexyl acetate [622-45-7] is very slightly miscible with water, but completely miscible with common organic solvents. Its solvency properties are comparable to those of amyl acetate. Cyclohexyl acetate dissolves oils, fats, resins, waxes, cellulose nitrate, cellulose tripropionate and acetobutyrate, alkyd resins, unsaturated and saturated polyester resins, phenolic resins and aminoplasts, poIy(vinyI chloride), vinyl chloride copolymers, poly(vinyl acetate), poly(vinyl ethers), epoxy resins, and acrylic resins, basic dyes, blown oils, crude rubber, metallic soaps, shellac, and bitumen. 

Aky (C8-10) glycldyl ether monomer, actuate coatings Bis l[[4-(ethenyloxy) methyl] cyclohexyl] melhyU terephthalate Bis (4-vinyl oxy huiyt) hexanedlylbiscarbamate monomer, acrylate/epoxy coatings VEctomer VE 4051 monomer, acrylic polymers Methylacrylate monomer, acrylic resins Butyl methacrylate Hydroxypropyl methacrylate Isobutyl methacrylate monomer, acrylics... 

Hydrogenated DGEBA. In 1976, Shell Chemical Co. introduced epoxy resins based on the diglycidyl ether of hydrogenated bisphenol A, 2,2-bis[4-(2,3-epoxypropoxy)cyclohexyl]propane (232-238 EEW rj at 25°C 2-2.5 Pa s). 

When one of the substituents is a ring, as in 4.23, another method is common. This could be named as cyclohexyl ethyl ether, but can also be described as ethoxycyclohexane. One rather special class of ethers is the epoxides, or oxiranes, such as 4.24 and 4.25. There are two methods by which they can be named—the first refers to the alkene from which they are generally synthesized plus the word oxide. Thus, 4.24 is ethene oxide and 4.25 cyclohexene oxide. Alternatively, the molecule may be named as an alkane, and then the word epoxy, and the location of the three-membered ring added. In this case, the names would be ethane epoxide and cyclohexane-l,2-epoxide. 

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