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  2. 4-Fluoroaniline - Wikipedia

    en.wikipedia.org/wiki/4-Fluoroaniline

    4-Fluoroaniline can be prepared by the hydrogenation of 4-nitrofluorobenzene. [2] It is a common building block in medicinal chemistry and related fields. [3] For example, it is a precursor to the fungicide fluoroimide or the fentanyl analogue parafluorofentanyl. It has also been evaluated for the production of ligands for homogeneous catalysis ...

  3. 4-Chloroaniline - Wikipedia

    en.wikipedia.org/wiki/4-Chloroaniline

    4-Chloroaniline is used in the industrial production of pesticides, drugs, and dyestuffs. It is a precursor to the widely used antimicrobial and bacteriocide chlorhexidine and is used in the manufacture of pesticides, including pyraclostrobin , anilofos , monolinuron , and chlorphthalim .

  4. 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.

  5. 4-Fluoronitrobenzene - Wikipedia

    en.wikipedia.org/wiki/4-Fluoronitrobenzene

    It is one of three isomeric fluoronitrobenzenes. [2] A yellow oil, it is prepared from 4-nitrochlorobenzene using the Halex process: O 2 NC 6 H 4 Cl + KF → O 2 NC 6 H 4 F + KCl. 4-Fluoronitrobenzene can be hydrogenated to give 4-fluoroaniline, [3] which is a precursor to the fungicide fluoroimide and parafluorofentanyl.

  6. Fluorous chemistry - Wikipedia

    en.wikipedia.org/wiki/Fluorous_chemistry

    The fluorous domain is often a substituent intended to confer solubility in the fluorocarbon medium. Such perfluorosubstituents are often introduced in what are called ponytails. Typical fluorous ponytails have the formula CF 3 (CF 2) n (CH 2) m - where n is about 10 and m is about 3. [1]

  7. Chloranil - Wikipedia

    en.wikipedia.org/wiki/Chloranil

    C 6 H 5 OH + 6 Cl 2 → C 6 Cl 6 O + 6 HCl C 6 Cl 6 O + H 2 O → C 6 Cl 4 O 2 + 2 HCl. Chloroanil serves as a hydrogen acceptor. It is more electrophilic than quinone itself. It is used for the aromatization reactions, such as the conversion of cyclohexadienes to the benzene derivatives. [4] Chloranil is used to test for free secondary amines.

  8. 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.

  9. Fluoroaniline - Wikipedia

    en.wikipedia.org/wiki/Fluoroaniline

    Fluoroaniline may refer to three compounds with the formula FC 6 H 4 NH 2: 2-Fluoroaniline; 3-Fluoroaniline; 4-Fluoroaniline

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