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  2. Cyclohexane (data page) - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane_(data_page)

    1 Material Safety Data Sheet. 2 Structure and properties. 3 Thermodynamic properties. ... Download as PDF; Printable version; In other projects Wikidata item; Appearance.

  3. Cyclohexanone - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanone

    Cyclohexanone is produced by the oxidation of cyclohexane in air, typically using cobalt catalysts: [11]. C 6 H 12 + O 2 → (CH 2) 5 CO + H 2 O. This process forms cyclohexanol as a by-product, and this mixture, called "KA Oil" for ketone-alcohol oil, is the main feedstock for the production of adipic acid.

  4. Cyclohexanone oxime - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanone_oxime

    Cyclohexanone oxime can be prepared from the condensation reaction between cyclohexanone and hydroxylamine: [1] C 5 H 10 CO + H 2 NOH → C 5 H 10 C=NOH + H 2 O. Alternatively, another industrial route involves the reaction of cyclohexane with nitrosyl chloride, which is a free-radical reaction. This method is advantageous as cyclohexane is ...

  5. Methylcyclohexanone - Wikipedia

    en.wikipedia.org/wiki/Methylcyclohexanone

    They can be viewed as derivative of cyclohexanone. They can be prepared by oxidation of methylcyclohexane as well as partial hydrogenation of the corresponding cresols. All are colorless liquids. The 2- and 3-isomers are chiral.

  6. Cyclohexane - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane

    Although rather unreactive, cyclohexane undergoes autoxidation to give a mixture of cyclohexanone and cyclohexanol. The cyclohexanone–cyclohexanol mixture, called "KA oil", is a raw material for adipic acid and caprolactam, precursors to nylon. Several million kilograms of cyclohexanone and cyclohexanol are produced annually. [9]

  7. 1,2-Cyclohexanedione - Wikipedia

    en.wikipedia.org/wiki/1,2-Cyclohexanedione

    It is a colorless compound that is soluble in a variety of organic solvents. It can be prepared by oxidation of cyclohexanone by selenium dioxide. [1] The enol is about 1 kcal/mol more stable than the diketo form. [2] Numerous diimine and dioxime ligands have been prepared from this diketone. [1] It also condenses with 1,2-diamines to give ...

  8. Cyclohexylbenzene - Wikipedia

    en.wikipedia.org/wiki/Cyclohexylbenzene

    Via the Hock rearrangement, cyclohexylbenzene hydroperoxide cleaves to give phenol and cyclohexanone: C 6 H 5 −C 6 H 10 OOH → C 6 H 5 OH + OC 6 H 10. Cyclohexanone is an important precursor to some nylons. [6] [3]

  9. Cyclohexanehexone - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanehexone

    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.

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