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  2. 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 .

  3. 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 ...

  4. 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 This page was last edited on 9 ...

  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. 4-Chloro-o-toluidine - Wikipedia

    en.wikipedia.org/wiki/4-Chloro-o-toluidine

    4-Chloro-o-toluidine (4-COT, 4-chloro-2-methylaniline) is the organic compound with the formula CH 3 C 6 H 3 Cl(NH 2). It is a colorless solid. It is a colorless solid. The compound is produced as an intermediate to the pesticide chlordimeform and a precursor to some azo dyes .

  7. Chlorobenzene (data page) - Wikipedia

    en.wikipedia.org/wiki/Chlorobenzene_(data_page)

    1 Material Safety Data Sheet. 2 Structure and properties. 3 Thermodynamic properties. 4 Vapor pressure of liquid. ... 633.4 K (360.25°C), 4.52 MPa Std enthalpy change

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  9. MCPA - Wikipedia

    en.wikipedia.org/wiki/MCPA

    The major metabolite of MCPA degradation is MCP (4-chloro-2-methylphenol). The pathway could be the cleavage of the ether linkage, yielding MCP and acetate acid. Another pathway could be the hydroxylation of the methyl group, yielding cloxyfonac (4-Chloro-2-hydroxymethylphenoxyacetic acid). Recent studies have demonstrated that biological ...

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