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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. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    Common names for ketones can be derived by naming the two alkyl or aryl groups bonded to the carbonyl group as separate words followed by the word ketone. Acetone; Acetophenone; Benzophenone; Ethyl isopropyl ketone; Diethyl ketone; The first three of the names shown above are still considered to be acceptable IUPAC names.

  4. Piceol - Wikipedia

    en.wikipedia.org/wiki/Piceol

    Chemical structure of piceol. Names Preferred IUPAC name. 1-(4-Hydroxyphenyl)ethan-1-one. Other names 1-(4-Hydroxyphenyl)ethanone 4-Hydroxyacetophenone

  5. Naproxen - Wikipedia

    en.wikipedia.org/wiki/Naproxen

    Naproxen's medical uses are related to its mechanism of action as an anti-inflammatory compound. [11] Naproxen is used to treat a variety of inflammatory conditions and symptoms that are due to excessive inflammation, such as pain and fever (naproxen has fever-reducing, or antipyretic, properties in addition to its anti-inflammatory activity). [11]

  6. Acetanisole - Wikipedia

    en.wikipedia.org/wiki/Acetanisole

    Its chemical names are based on considering the structure as either an acetyl (methyl-ketone) analog of anisole. Other names It can also be seen as a methyl ether analog of acetophenone. Acetanisole is found naturally in castoreum, the glandular secretion of the beaver. [1]

  7. Phenacyl chloride - Wikipedia

    en.wikipedia.org/wiki/Phenacyl_chloride

    Phenacyl chloride, also commonly known as chloroacetophenone, is a substituted acetophenone.It is a useful building block in organic chemistry.Apart from that, it has been historically used as a riot control agent, where it is designated CN. [5]

  8. Phenylacetone - Wikipedia

    en.wikipedia.org/wiki/Phenylacetone

    As such, its systematic IUPAC name is 1-phenyl-2-propanone. This substance is used in the manufacture of methamphetamine and amphetamine , where it is commonly known as P2P . [ 2 ] [ 3 ] Due to illicit drug labs using phenylacetone to make amphetamines, phenylacetone was declared a schedule II controlled substance in the United States in 1980 ...

  9. Phenacyl bromide - Wikipedia

    en.wikipedia.org/wiki/Phenacyl_bromide

    Names Preferred IUPAC name. 2-Bromo-1-phenylethan-1-one. Other names ... It is prepared by bromination of acetophenone: [2] C 6 H 5 C(O)CH 3 + Br 2 → C 6 H 5 C(O)CH ...