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  2. Fluorobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/Fluorobenzaldehyde

    Fluorobenzaldehyde isomers Name o-Fluorobenzaldehyde m-Fluorobenzaldehyde p-Fluorobenzaldehyde Structure: Systematic name: 2-Fluorobenzaldehyde 3-Fluorobenzaldehyde 4-Fluorobenzaldehyde Molecular formula: C 7 H 5 FO C 7 H 5 FO C 7 H 5 FO Molar mass: 124.11 g/mol 124.11 g/mol 124.11 g/mol CAS number: 446-52-6 456-48-4 459-57-4 EC number 207-171 ...

  3. 4-Chlorobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/4-Chlorobenzaldehyde

    4-Chlorobenzaldehyde (o-Chlorobenzaldehyde) is an organic compound with the formula ClC 5 H 4 CHO. It is one of three isomeric monochlorinated benzaldehydes . Preparation

  4. 2-Chlorobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/2-Chlorobenzaldehyde

    2-Chlorobenzaldehyde (o-chlorobenzaldehyde) is an organic compound with the formula ClC 5 H 4 CHO. It is one of three isomeric monochlorinated benzaldehyde. 3-Chlorobenzaldehyde and 4-chlorobenzaldehyde are the other isomers. Whereas benzaldehyde is prone to autoxidation, the 2-chloro derivatives are more air-stable.

  5. 2-Chloro-6-fluorobenzaldehyde - Wikipedia

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

    2-Chloro-6-fluorobenzaldehyde is prepared by oxidation of 2-chloro-6-fluorotolulene by chromyl chloride. [3] It reacts with sodium hydroxide to give a mixture of 2-chloro-6-fluorobenzene and 6-chlorosalicaldehyde. [4] 2-Chloro-6-fluorobenzaldehyde is used in the production of the antiseptics dicloxacillin and flucloxacillin.

  6. Chlorofluorocarbon - Wikipedia

    en.wikipedia.org/wiki/Chlorofluorocarbon

    An easy example is that of CFC-12, which gives: 90+12=102 -> 1 carbon, 0 hydrogens, 2 fluorine atoms, and hence 2 chlorine atoms resulting in CCl 2 F 2. The main advantage of this method of deducing the molecular composition in comparison with the method described in the paragraph above is that it gives the number of carbon atoms of the molecule.

  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. 2-Chloro-6-fluorotoluene - Wikipedia

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

    CFT is used to prepare 2-chloro-6-fluorobenzaldehyde via oxidation with hydrogen peroxide, which forms an aldehyde group. [ 2 ] CFT is also used in the preparation of 4-chloro-1 H -indazole .

  9. Chlorofluoromethane - Wikipedia

    en.wikipedia.org/wiki/Chlorofluoromethane

    Chlorofluoromethane or Freon 31 is the hydrochlorofluorocarbon (HCFC) with the formula CH 2 ClF. It is a colorless, odorless, flammable gas. [ 1 ] It is a class II ozone depleting substance and in accordance with the montreal protocol, its production and import were banned on 1 January 2015.

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