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  2. Cyclohexanone oxime - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanone_oxime

    Melting point: 88 to 91 °C (190 to 196 °F; 361 to 364 K) Boiling point: ... Cyclohexanone oxime is an organic compound containing the functional group oxime.

  3. Cyclohexanone - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanone

    Melting point: −47 °C (−53 ... Cyclohexanone is the organic compound with the ... The other half of the cyclohexanone supply is converted to cyclohexanone oxime.

  4. Isobutyric anhydride - Wikipedia

    en.wikipedia.org/wiki/Isobutyric_anhydride

    Melting point: −53.5 °C (−64.3 °F; 219.7 K) ... Isobutyric anhydride is a reagent in the production of the ester of cyclohexanone oxime. [5] Applications

  5. Oxime - Wikipedia

    en.wikipedia.org/wiki/Oxime

    In organic chemistry, an oxime is an organic compound belonging to the imines, with the general formula RR’C=N−OH, where R is an organic side-chain and R' may be hydrogen, forming an aldoxime, or another organic group, forming a ketoxime. O-substituted oximes form a closely related family of compounds.

  6. N-Hydroxyphthalimide - Wikipedia

    en.wikipedia.org/wiki/N-Hydroxyphthalimide

    The use of N-hydroxyphthalimide as a catalyst in the oxidation of KA oil avoids the formation of the undesirable by-product ammonium sulfate which is produced by the conventional ε-caprolactam synthesis (Beckmann rearrangement of cyclohexanone oxime with sulfuric acid). Alkanes are converted into nitroalkanes in the presence of nitrogen ...

  7. Cyclohexanol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanol

    Cyclohexanol is produced by the oxidation of cyclohexane in air, typically using cobalt catalysts: [5]. 2 C 6 H 12 + O 2 → 2 C 6 H 11 OH. This process coforms cyclohexanone, and this mixture ("KA oil" for ketone-alcohol oil) is the main feedstock for the production of adipic acid.

  8. Hydroxylamine - Wikipedia

    en.wikipedia.org/wiki/Hydroxylamine

    Conversion of cyclohexanone to caprolactam involving the Beckmann rearrangement. Approximately 95% of hydroxylamine is used in the synthesis of cyclohexanone oxime , a precursor to Nylon 6 . [ 10 ] The treatment of this oxime with acid induces the Beckmann rearrangement to give caprolactam ( 3 ). [ 21 ]

  9. Cyclohexenone - Wikipedia

    en.wikipedia.org/wiki/Cyclohexenone

    It can be obtained from cyclohexanone by α-bromination followed by treatment with base. Hydrolysis of 3-chloro cyclohexene followed by oxidation of the cyclohexenol is yet another route. Cyclohexenone is produced industrially by catalytic oxidation of cyclohexene, for example with hydrogen peroxide and vanadium catalysts. Several patents ...