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In recent times the catalytic oxidation of cyclohexene by (immobilized) metalloporphyrin complexes has been found to be an efficient way. [7] [8] In laboratory, cyclohexene oxide can also be prepared by reacting cyclohexene with magnesium monoperoxyphthalate (MMPP) in a mixture of isopropanol and water as solvent at room temperature. [9]
cyclohexene oxide: 286-20-4 C 6 H 10 O: hexenal: 1335-39-3 C 6 H 10 O: meparfynol: 77-75-8 C 6 H 10 OS: allyl thiopropionate: 41820-22-8 C 6 H 10 OS 2: allicin: 539-86-6 C 6 H 10 O 2: cyclobutanecarboxylic acid methyl ester: 765-85-5 C 6 H 10 O 2: cyclobutyl ethanoate: 500033-42-1 C 6 H 10 O 2: cyclopentane carboxylic acid: 3400-45-1 C 6 H 10 O ...
Benzene is converted to cyclohexylbenzene by acid-catalyzed alkylation with cyclohexene. [6] Cyclohexylbenzene is a precursor to both phenol and cyclohexanone. [7] Hydration of cyclohexene gives cyclohexanol, which can be dehydrogenated to give cyclohexanone, a precursor to caprolactam. [8] The oxidative cleavage of cyclohexene gives adipic acid.
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IUPAC names can sometimes be simpler than older names, as with ethanol, instead of ethyl alcohol. For relatively simple molecules they can be more easily understood than non-systematic names, which must be learnt or looked over. However, the common or trivial name is often substantially shorter and clearer, and so preferred. These non ...
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Cyclohexanehexone, also known as hexaketocyclohexane and triquinoyl, is an organic compound with formula C 6 O 6, the sixfold ketone of cyclohexane.It is an oxide of carbon (an oxocarbon), a hexamer of carbon monoxide.
4-Vinylcyclohexene is an organic compound consisting of a vinyl group attached to the 4-position of the cyclohexene ring. It is a colorless liquid. Although chiral, it is used mainly as the racemate. It is a precursor to vinylcyclohexene dioxide. [4]