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  2. Acetophenone - Wikipedia

    en.wikipedia.org/wiki/Acetophenone

    Acetophenone is formed as a byproduct of the cumene process, the industrial route for the synthesis of phenol and acetone.In the Hock rearrangement of isopropylbenzene hydroperoxide, migration of a methyl group rather than the phenyl group gives acetophenone and methanol as a result of an alternate rearrangement of the intermediate:

  3. Ketone - Wikipedia

    en.wikipedia.org/wiki/Ketone

    Acetophenone (C 6 H 5 C(O)CH 3) is an unsymmetrical ketone. Diketones. Many kinds of diketones are known, some with unusual properties. The simplest is ...

  4. Piceol - Wikipedia

    en.wikipedia.org/wiki/Piceol

    Piceol is used in the synthesis of several pharmaceutical drugs including octopamine, sotalol, bamethan, and dyclonine. [citation needed] Piceol can be used to make acetaminophen by condensation with hydroxylamine and subsequent Beckmann rearrangement in acid. [4] Anticonvulsants are also possible by Mannich reaction: [5]

  5. Phenacyl bromide - Wikipedia

    en.wikipedia.org/wiki/Phenacyl_bromide

    Properties Chemical formula. C 8 H 7 Br O: Molar mass: 199.047 g·mol −1 ... It is prepared by bromination of acetophenone: [2] C 6 H 5 C(O)CH 3 + Br 2 → C 6 H 5 ...

  6. Acetone - Wikipedia

    en.wikipedia.org/wiki/Acetone

    Acetone is a good solvent for many plastics and some synthetic fibers. It is used for thinning polyester resin, cleaning tools used with it, and dissolving two-part epoxies and superglue before they harden. It is used as one of the volatile components of some paints and varnishes.

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  8. Category:Acetophenones - Wikipedia

    en.wikipedia.org/wiki/Category:Acetophenones

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