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  2. 4-Chlorobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/4-Chlorobenzaldehyde

    It can be produced by hydrolysis of 4-chlorobenzal chloride: [2]. ClC 5 H 4 CHCl 2 + H 2 O → ClC 5 H 4 CHO + 2 HCl. It can also be produced by the oxidation of 4-chlorobenzyl alcohol.

  3. Benzal chloride - Wikipedia

    en.wikipedia.org/wiki/Benzal_chloride

    Benzal chloride is an organic compound with the formula C 6 H 5 CHCl 2. [1] This colourless liquid is a lachrymator and is used as a building block in organic synthesis . Preparation and usage

  4. Chlorobenzene - Wikipedia

    en.wikipedia.org/wiki/Chlorobenzene

    Chlorobenzene (abbreviated PhCl) is an aryl chloride and the simplest of the chlorobenzenes, consisting of a benzene ring substituted with one chlorine atom. Its chemical formula is C 6 H 5 Cl. This colorless, flammable liquid is a common solvent and a widely used intermediate in the manufacture of other chemicals.

  5. Benzyl chloride - Wikipedia

    en.wikipedia.org/wiki/Benzyl_chloride

    Industrially, benzyl chloride is the precursor to benzyl esters, which are used as plasticizers, flavorants, and perfumes. Phenylacetic acid, a precursor to pharmaceuticals, is produced from benzyl cyanide, which in turn is generated by treatment of benzyl chloride with sodium cyanide.

  6. 4,4'-Dichlorobenzophenone - Wikipedia

    en.wikipedia.org/wiki/4,4'-dichlorobenzophenone

    4,4’-Dichlorobenzophenone is prepared by the acylation of chlorobenzene with 4-chlorobenzoyl chloride. The conversion is typically conducted in the presence of an aluminium chloride catalyst in a petroleum ether solvent. ClC 6 H 5 C(O)Cl + C 6 H 5 Cl → (ClC 6 H 4) 2 CO + HCl

  7. Benzyl chloroformate - Wikipedia

    en.wikipedia.org/wiki/Benzyl_chloroformate

    Benzyl chloroformate, also known as benzyl chlorocarbonate or Z-chloride, is the benzyl ester of chloroformic acid. It can be also described as the chloride of the benzyloxycarbonyl (Cbz or Z) group. In its pure form it is a water-sensitive oily colorless liquid, although impure samples usually appear yellow.

  8. Benzoyl group - Wikipedia

    en.wikipedia.org/wiki/Benzoyl_group

    The benzoyl functional group.. In organic chemistry, benzoyl (/ ˈ b ɛ n z oʊ ɪ l /, BENZ-oh-il) [1] is the functional group with the formula −COC 6 H 5 and structure −C(=O)−C 6 H 5. [2] [3] It can be viewed as benzaldehyde missing one hydrogen.

  9. 4-chlorobenzoyl-CoA dehalogenase - Wikipedia

    en.wikipedia.org/wiki/4-chlorobenzoyl-CoA_de...

    In enzymology, a 4-chlorobenzoyl-CoA dehalogenase (EC 3.8.1.7) is an enzyme that catalyzes the chemical reaction. 4-chlorobenzoyl-CoA + H 2 O 4-hydroxybenzoyl CoA + chloride. Thus, the two substrates of this enzyme are 4-chlorobenzoyl-CoA and H 2 O, whereas its two products are 4-hydroxybenzoyl CoA and chloride.