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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...

    Commas are put between numbers (2 5 5 becomes 2,5,5) Hyphens are put between a number and a letter (2 5 5 trimethylheptane becomes 2,5,5-trimethylheptane) Successive words are merged into one word (trimethyl heptane becomes trimethylheptane) Note: IUPAC uses one-word names throughout. This is why all parts are connected. The resulting name ...

  4. Piceol - Wikipedia

    en.wikipedia.org/wiki/Piceol

    Piceol is a phenolic compound found in the needles and in mycorrhizal roots of Norway spruces (Picea abies). [ 1 ] [ 2 ] Picein is the glucoside of piceol. [ 3 ]

  5. 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]

  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. Cumene hydroperoxide - Wikipedia

    en.wikipedia.org/wiki/Cumene_hydroperoxide

    Cumene hydroperoxide is the organic compound with the formula C 6 H 5 C(CH 3) 2 OOH; this oily liquid is classified as an organic hydroperoxide. [2] Products of decomposition of cumene hydroperoxide are methylstyrene, acetophenone, and 2-phenylpropan-2-ol. [3] It is produced by treatment of cumene with oxygen, an autoxidation.

  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. Acetanisole - Wikipedia

    en.wikipedia.org/wiki/Acetanisole

    Acetanisole is an aromatic chemical compound with an aroma described as sweet, fruity, nutty, and similar to vanilla. In addition acetanisole can sometimes smell like butter or caramel. [ 3 ] Its chemical names are based on considering the structure as either an acetyl ( methyl - ketone ) analog of anisole .