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  2. Cyclohexene - Wikipedia

    en.wikipedia.org/wiki/Cyclohexene

    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.

  3. Chemical safety assessment - Wikipedia

    en.wikipedia.org/wiki/Chemical_Safety_Assessment

    Chemical Safety Reports are the main end point for data assessment under REACH (the European Community Regulation on chemicals and their safe use, concerning the Registration, Evaluation, Authorisation and Restriction of Chemical substances [4]) in which hazard and exposure data are considered together to assess the risk of a substance. [5]

  4. Cyclohexylbenzene - Wikipedia

    en.wikipedia.org/wiki/Cyclohexylbenzene

    Cyclohexylbenzene is now industrially produced by the acid-catalyzed alkylation of benzene with cyclohexene. [ 3 ] [ 4 ] The process can proceed using benzene as the exclusive organic precursor. Its partial hydrogenation gives cyclohexene, which alkylates the unhydrogenated benzene.

  5. 4-Methylcyclohexene - Wikipedia

    en.wikipedia.org/wiki/4-Methylcyclohexene

    4-Methylcyclohexene is an organic compound consisting of cyclohexene with a methyl group substituent attached to carbon most distant from the alkene group. Two other structural isomers are known: 1-methylcyclohexene and 3-methylcyclohexene. All are colorless volatile liquids classified as a cyclic olefins. They are specialized reagents.

  6. Cyclohexene oxide - Wikipedia

    en.wikipedia.org/wiki/Cyclohexene_oxide

    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]

  7. 4-Vinylcyclohexene - Wikipedia

    en.wikipedia.org/wiki/4-Vinylcyclohexene

    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]

  8. 1-Methylcyclohexene - Wikipedia

    en.wikipedia.org/wiki/1-Methylcyclohexene

    1-Methylcyclohexene an organic compound consisting of cyclohexene with a methyl group substituent attached to the alkene group. Two other structural isomers are known: 3-methylcyclohexene and 4-methylcyclohexene. All are colorless volatile liquids. They are specialized reagents.

  9. Cyclohexadiene - Wikipedia

    en.wikipedia.org/wiki/Cyclohexadiene

    Cyclohexene This page was last edited on 25 June 2024, at 09:29 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4.0 ...