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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. Category:4-Chlorophenyl compounds - Wikipedia

   en.wikipedia.org/wiki/Category:4-Chlorophenyl...

   Pages in category "4-Chlorophenyl compounds" The following 200 pages are in this category, out of approximately 257 total. This list may not reflect recent changes .

4. 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. The compound is produced as an intermediate to the pesticide chlordimeform and a precursor to some azo dyes. Production has declined after it was shown to be highly carcinogenic.

5. List of insecticides - Wikipedia

   en.wikipedia.org/wiki/List_of_insecticides

   The industry-sponsored Insecticide Resistance Action Committee (IRAC) advises on the use of insecticides in crop protection and classifies the available compounds according to their chemical structures and mechanism of action so as to manage the risks of pesticide resistance developing. [4] The 2024 IRAC poster of insecticide modes of action ...

6. Organochlorine chemistry - Wikipedia

   en.wikipedia.org/wiki/Organochlorine_chemistry

   Some organochlorides are considered safe enough for consumption in foods and medicines. For example, peas and broad beans contain the natural chlorinated plant hormone 4-chloroindole-3-acetic acid (4-Cl-IAA); [15] [16] and the sweetener sucralose (Splenda) is widely used in diet products.

7. 4,7-Dichloroquinoline - Wikipedia

   en.wikipedia.org/wiki/4,7-Dichloroquinoline

   4,7-Dichloroquinoline was first reported in a patent filed by IG Farben in 1937. [2] However, its synthesis was not investigated in detail until chloroquine was developed as an antimalarial drug. [ 3 ] : 130–132 A route to the intermediate starting from 3-chloroaniline was developed by chemists at Winthrop Chemical Co .