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  2. Diethylbenzenes - Wikipedia

    en.wikipedia.org/wiki/Diethylbenzenes

    Diethylbenzenes arise as side-products of the alkylation of benzene with ethylene, which can be described as two steps. The first step is the industrial route to ethylbenzene, which is produced on a large scale as a precursor to styrene.

  3. Xylene - Wikipedia

    en.wikipedia.org/wiki/Xylene

    The three xylene isomers: o-xylene, m-xylene, and p-xylene In organic chemistry, xylene or xylol (from Greek ξύλον (xylon) 'wood'; [1] [2] IUPAC name: dimethylbenzene) are any of three organic compounds with the formula (CH 3) 2 C 6 H 4.

  4. 3-Quinuclidinyl benzilate - Wikipedia

    en.wikipedia.org/wiki/3-Quinuclidinyl_benzilate

    As a powerful anticholinergic agent, BZ produces a syndrome of effects known as the anticholinergic toxidrome: these include both psychological and physiological effects, with the most incapacitating effect being a state of delirium characterized by cognitive dysfunction, hallucinations, and inability to perform basic tasks.

  5. DEA list of chemicals - Wikipedia

    en.wikipedia.org/wiki/DEA_list_of_chemicals

    The United States Drug Enforcement Administration (DEA) maintains lists regarding the classification of illicit drugs (see DEA Schedules).It also maintains List I of chemicals and List II of chemicals, which contain chemicals that are used to manufacture the controlled substances/illicit drugs.

  6. C4-Benzenes - Wikipedia

    en.wikipedia.org/wiki/C4-Benzenes

    The C 4-benzenes are a class of organic aromatic compounds which contain a benzene ring and four other carbon atoms. There are three tetramethylbenzenes, six dimethylethylbenzenes, three diethylbenzenes, three isopropylmethylbenzenes, three n-propylmethylbenzenes and four butylbenzenes.

  7. Divinylbenzene - Wikipedia

    en.wikipedia.org/wiki/Divinylbenzene

    It is produced by dehydrogenation of diethylbenzene: C 6 H 4 (C 2 H 5) 2 → C 6 H 4 (C 2 H 3) 2 + 2 H 2. Divinylbenzene is usually encountered as a 2:1 mixture of m- and p-divinylbenzene, containing also the corresponding isomers of ethylvinylbenzene. Styrene and divinylbenzene react to form the copolymer styrene-divinylbenzene, S-DVB or Sty-DVB.

  8. Toluene - Wikipedia

    en.wikipedia.org/wiki/Toluene

    Toluene (/ ˈ t ɒ l. j u iː n /), also known as toluol (/ ˈ t ɒ l. j u. ɒ l,-ɔː l,-oʊ l /), is a substituted aromatic hydrocarbon [15] with the chemical formula C 6 H 5 CH 3, often abbreviated as PhCH 3, where Ph stands for the phenyl group.

  9. Diethynylbenzene dianion - Wikipedia

    en.wikipedia.org/wiki/Diethynylbenzene_dianion

    In organic chemistry, a diethynylbenzene dianion is an anion consisting of two ethynyl anions as substituents on a benzene ring. With the chemical formula C 6 H 4 C 2− 4, three positional isomers are possible, differing in the relative positions of the two substituents around the ring: