enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  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...

    To avoid long and tedious names in normal communication, the official IUPAC naming recommendations are not always followed in practice, except when it is necessary to give an unambiguous and absolute definition to a compound. IUPAC names can sometimes be simpler than older names, as with ethanol, instead of ethyl alcohol. For relatively simple ...

  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. 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. 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 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 ...

  8. Naproxen - Wikipedia

    en.wikipedia.org/wiki/Naproxen

    Naproxen is not contraindicated in the presence of SSRIs, though concomitant use of the medications should be done with caution. [32] Alcohol consumption increases the risk of gastrointestinal bleeding when combined with NSAIDs like naproxen in a dose-dependent manner (that is, the higher the dose of naproxen, the higher the risk of bleeding). [33]

  9. 1-Phenylethanol - Wikipedia

    en.wikipedia.org/wiki/1-phenylethanol

    1-Phenylethanol is the organic compound with the formula C 6 H 5 CH(OH)CH 3. It is one of the most commonly available chiral alcohols. It is a colorless liquid with a mild gardenia-hyacinth scent. [4] Phenylethanol is an aromatic alcohol, it has the role of mouse metabolite.