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  2. Acetophenone - Wikipedia

    en.wikipedia.org/wiki/Acetophenone

    Acetophenone is the organic compound with the formula C 6 H 5 C(O)CH 3. It is the simplest aromatic ketone . This colorless, viscous liquid is a precursor to useful resins and fragrances.

  3. Piceol - Wikipedia

    en.wikipedia.org/wiki/Piceol

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us

  4. 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]

  5. Aspirin - Wikipedia

    en.wikipedia.org/wiki/Aspirin

    [149] [150] Naproxen has been shown to be as effective as aspirin and less toxic, but due to the limited clinical experience, naproxen is recommended only as a second-line treatment. [ 149 ] [ 151 ] Along with rheumatic fever, Kawasaki disease remains one of the few indications for aspirin use in children [ 152 ] in spite of a lack of high ...

  6. 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]

  7. 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 .

  8. Phenacyl bromide - Wikipedia

    en.wikipedia.org/wiki/Phenacyl_bromide

    Phenacyl bromide is the organic compound with the formula C 6 H 5 C(O)CH 2 Br. This colourless solid is a powerful lachrymator as well as a useful precursor to other organic compounds. 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 2 Br + HBr. The compound was first reported in 1871. [3]

  9. Phenylglyoxal - Wikipedia

    en.wikipedia.org/wiki/Phenylglyoxal

    Phenylglyoxal was first prepared by thermal decomposition of the sulfite derivative of the oxime: [5]. C 6 H 5 C(O)CH(NOSO 2 H) + 2 H 2 O → C 6 H 5 C(O)CHO + NH 4 HSO 4. More conveniently, it can be prepared from methyl benzoate by reaction with KCH 2 S(O)CH 3 to give PhC(O)CH(SCH 3)(OH), which is oxidized with copper(II) acetate. [6]

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