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  2. Acetophenone - Wikipedia

    en.wikipedia.org/wiki/Acetophenone

    C 6 H 5 C(CH 3) 2 O 2 H → C 6 H 5 C(O)CH 3 + CH 3 OH. The cumene process is conducted on such a large scale that even the small amount of acetophenone by-product can be recovered in commercially useful quantities. [2] Acetophenone is also generated from ethylbenzene hydroperoxide.

  3. IUPAC nomenclature of organic chemistry - Wikipedia

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

    For example, the three isomers of xylene CH 3 C 6 H 4 CH 3, commonly the ortho-, meta-, and para-forms, are 1,2-dimethylbenzene, 1,3-dimethylbenzene, and 1,4-dimethylbenzene. The cyclic structures can also be treated as functional groups themselves, in which case they take the prefix "cyclo alkyl -" (e.g. "cyclohexyl-") or for benzene, "phenyl-".

  4. Piceol - Wikipedia

    en.wikipedia.org/wiki/Piceol

    Chemical structure of piceol. Names Preferred IUPAC name. 1-(4-Hydroxyphenyl)ethan-1-one. ... [1] [2] Picein is the glucoside of piceol. [3] Uses

  5. Naproxen - Wikipedia

    en.wikipedia.org/wiki/Naproxen

    OTC preparations of naproxen in the U.S. are mainly marketed by Bayer HealthCare under the brand name Aleve and generic store brand formulations in 220 mg tablets. [44] In Australia, packets of 275 mg tablets of naproxen sodium are Schedule 2 pharmacy medicines , with a maximum daily dose of five tablets or 1375 mg.

  6. Tetramethyl acetyloctahydronaphthalenes - Wikipedia

    en.wikipedia.org/wiki/Tetramethyl_acetylocta...

    Tetramethyl acetyloctahydronaphthalenes (International Nomenclature for Cosmetic Ingredients name) (1-(1,2,3,4,5,6,7,8-ottaidro-2,3,8,8,-tetrametil-2-naftil)etan-1-one) is a synthetic ketone fragrance also known as OTNE (octahydrotetramethyl acetophenone) and by other commercial trade names such as: Iso E Super, Iso Gamma Super, Anthamber, Amber Fleur, Boisvelone, Iso Ambois, Amberlan, Iso ...

  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. IUPAC polymer nomenclature - Wikipedia

    en.wikipedia.org/wiki/IUPAC_polymer_nomenclature

    In the example, there is a bromo-substituted -CH 2-CH 2 - subunit. 1-Bromoethane-1,2-diyl is chosen in preference to 2- bromoethane-1,2-diyl as the former has a lower locant for the bromo-substituent. The preferred CRU is therefore oxy(1-bromoethane-1,2-diyl) and the polymer is thus named poly[oxy(1-bromoethane-1,2-diyl)].

  9. Acetanisole - Wikipedia

    en.wikipedia.org/wiki/Acetanisole

    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. 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]

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