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  2. Cyclohexylbenzene - Wikipedia

    en.wikipedia.org/wiki/Cyclohexylbenzene

    A route to phenol analogous to the cumene process begins with cyclohexylbenzene, which is oxidized to a hydroperoxide, akin to the production of cumene hydroperoxide. 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

  3. Cumene process - Wikipedia

    en.wikipedia.org/wiki/Cumene_process

    Cyclohexylbenzene can replace isopropylbenzene. Via the Hock rearrangement, cyclohexylbenzene hydroperoxide cleaves to give phenol and cyclohexanone. Cyclohexanone is an important precursor to some nylons. [8] Starting with the alkylation of benzene with mixture of 1 and 2-butenes, the cumene process produces phenol and butanones. [5]

  4. Phenol - Wikipedia

    en.wikipedia.org/wiki/Phenol

    Phenol is also a versatile precursor to a large collection of drugs, most notably aspirin but also many herbicides and pharmaceutical drugs. Phenol is a component in liquid–liquid phenol–chloroform extraction technique used in molecular biology for obtaining nucleic acids from tissues or cell culture samples.

  5. 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.

  6. Phenols - Wikipedia

    en.wikipedia.org/wiki/Phenols

    Phenol esters are active esters, being prone to hydrolysis. Phenols are reactive species toward oxidation . Oxidative cleavage, for instance cleavage of 1,2-dihydroxybenzene to the monomethylester of 2,4 hexadienedioic acid with oxygen, copper chloride in pyridine [ 4 ] Oxidative de-aromatization to quinones also known as the Teuber reaction .

  7. Dictionary of natural phenols and polyphenols molecular ...

    en.wikipedia.org/wiki/Dictionary_of_natural...

    2,4-Bis(4-hydroxybenzyl) phenol 306.125594 C16H20O6: Monocerin 308.1259876 C13H12O9: Caftaric acid 312.048132 C13H16O9: Norbergenin 314.063782 C17H14O6: Ermanin, others 314.079038 C18H18O5: Flavokavain A, others 314.115424 C17H15O6: Rosinidin 315.086863 C16H12O7: Isorhamnetin, others 316.058303 C19H24O4: Ferujol 316.167459 C18H20O5 ...

  8. Cyclohexenone - Wikipedia

    en.wikipedia.org/wiki/Cyclohexenone

    Industrially, cyclohexenone is prepared from phenol by Birch reduction. [3] Cyclohexenone is a ketone, or more precisely an enone. Common reactions include nucleophilic conjugate addition with organocopper reagents, Michael reactions and Robinson annulations. [4] [5]

  9. Category:Phenyl compounds - Wikipedia

    en.wikipedia.org/wiki/Category:Phenyl_compounds

    P. Pentafluorosulfanylbenzene; Pentaphenylphosphorus; Perchlorylbenzene; Peroxybenzoic acid; Phanephos; Phenatine; Phenethyl alcohol; Phenethyl isothiocyanate