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2,4,6-Trichlorophenol, also known as TCP, phenaclor, Dowicide 2S, Dowcide 2S, omal, is a chlorinated phenol that has been used as a fungicide, herbicide, insecticide, antiseptic, [3] defoliant, and glue preservative. [4] It is a clear to yellowish crystalline solid with a strong, phenolic odor.
Different isomers of trichlorophenol exist according to which ring positions on the phenol contain chlorine atoms. 2,4,6-Trichlorophenol, for example, has two chlorine atoms in the ortho positions and one chlorine atom in the para position. There are six different isomers: 2,3,4-Trichlorophenol; 2,3,5-Trichlorophenol; 2,3,6-Trichlorophenol
C 6 H 2 Cl 3 NO 2,6-Dichloroquinone-4-chloroimideGibbs reagent C 6 H 3 Br 3 O: 2,4,6-Tribromophenol: C 6 H 3 Cl 3 O: 2,4,6-Trichlorophenol: C 6 H 4 BrNO 2: 5-bromonicotinic acid: 20826-04-4 C 6 H 4 ClNO 2: 2-chloronicotinic acid: 2942-59-8 C 6 H 4 ClN 3: 4-Chlorophenyl azide: C 6 H 4 ClNO 2: 6-chloro-2-pyridinecarboxylic acid: 4684-94-0 6 ...
13775–53–6 Na 3 Co(NO 2) 6: sodium cobaltnitrite: 14649–73–1 Na 3 PO 4: sodium phosphate: 7601–54–9 Na 3 Sb: sodium antimonide: 12058–86–5 Na 3 SbS 4: sodium thioantimonide: 13776–84–6 Na 3 VO 4: sodium vanadate: 13721–39–6 Na 4 C 4 H 4 O 6: sodium tartrate: 868–18–8 Na 4 FeC 6 N 6: sodium ferrocyanide: 13601–19 ...
The chlorophenol precursor, 2,4,6-trichlorophenol, is used as a fungicide; more generally, related compounds can originate as contaminants found in some pesticides and wood preservatives, or as by-products of the chlorine bleaching process used to sterilize or bleach wood, paper, and other materials.
Chemical structure of 2-chlorophenol. A chlorophenol is any organochloride of phenol that contains one or more covalently bonded chlorine atoms. There are five basic types of chlorophenols (mono- to pentachlorophenol) and 19 different chlorophenols in total when positional isomerism is taken into account.
A tetrachlorophenol is any organochloride of phenol that contains four covalently bonded chlorine atoms. Tetrachlorophenols are produced by electrophilic halogenation of phenol with chlorine. [1]
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