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  2. Chlorotoluene - Wikipedia

    en.wikipedia.org/wiki/Chlorotoluene

    A laboratory route to 2- and 4-chlorotoluene proceeds from 2- and 4-toluidines (i.e. 2- and 4-aminotoluene). These compounds are diazotized followed by treatment with cuprous chloride. [1] Industrially, the diazonium method is reserved for 3-chlorotoluene. The industrial route to 2- and 4-chlorotoluene entails direct reaction of toluene with ...

  3. Ethyltoluene - Wikipedia

    en.wikipedia.org/wiki/Ethyltoluene

    Ethyltoluene describes organic compounds with the formula CH 3 C 6 H 4 CH 2 CH 3. Three isomers exist: 1,2- 1,3-, and 1,4-. All are colorless liquids, immiscible in water, with similar boiling points. They are classified are aromatic hydrocarbons. The ring bears two substituents: a methyl group and an ethyl group. [1]

  4. 2-Chloro-6-fluorotoluene - Wikipedia

    en.wikipedia.org/wiki/2-Chloro-6-fluorotoluene

    2-Chloro-6-fluorotoluene (CFT) is a halogenated derivative of toluene that is used as an intermediate in numerous organic syntheses. [1] [2] Uses.

  5. Dichlorotoluene - Wikipedia

    en.wikipedia.org/wiki/Dichlorotoluene

    Purification is challenging because the individual isomers have similar properties. The 2,6 and 3,5 isomers do not form acceptably from toluene or chlorotoluenes, so these isomers are prepared by indirect methods. For example, 2,6-dichlorotoluene can be prepared by chlorination of 4-toluenesulfonyl chloride followed by desulfonation. [1]

  6. 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.

  7. Organochlorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organochlorine_chemistry

    H 2 C=CH 2 + HCl → CH 3 CH 2 Cl. In oxychlorination, hydrogen chloride instead of the more expensive chlorine is used for the same purpose: CH 2 =CH 2 + 2 HCl + 1 ⁄ 2 O 2 → ClCH 2 CH 2 Cl + H 2 O. Secondary and tertiary alcohols react with hydrogen chloride to give the corresponding chlorides.

  8. Chloroethyl chloroformate - Wikipedia

    en.wikipedia.org/wiki/Chloroethyl_chloroformate

    Chloroethyl chloroformates (chemical formula: C 3 H 4 Cl 2 O 2) are a pair of related chemical compounds. They can be used to form protecting groups and as N-dealkylating agents. [1] They are listed as extremely hazardous substances. [2]

  9. Odor detection threshold - Wikipedia

    en.wikipedia.org/wiki/Odor_detection_threshold

    The odor detection threshold is the lowest concentration of a certain odor compound that is perceivable by the human sense of smell.The threshold of a chemical compound is determined in part by its shape, polarity, partial charges, and molecular mass.