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A trichlorophenol is any organochloride of phenol that contains three covalently bonded chlorine atoms. Trichlorophenols are produced by electrophilic halogenation of phenol with chlorine. [ 1 ] Different isomers of trichlorophenol exist according to which ring positions on the phenol contain chlorine atoms.
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.
Monochlorophenols have three isomers because there is only one chlorine atom that can occupy one of three ring positions on the phenol molecule; 2-chlorophenol, for example, is the isomer that has a chlorine atom in the ortho position.
2,4,5-Trichlorophenol (TCP) is an organochloride with the molecular formula C 6 H 3 Cl 3 O.It has been used as a fungicide and herbicide. [2] Precursor chemical used in the production of 2,4,5-Trichlorophenoxyacetic acid (2,4,5-T) and hexachlorophene involves the intermediate production of 2,4,5-trichlorophenol (TCP) and the formation of 2,3,7,8-Tetrachlorodibenzodioxin (TCDD, commonly ...
It is the symmetric isomer of trichloroanisole. It is a colorless solid. ... The chlorophenol precursor, 2,4,6-trichlorophenol, is used as a fungicide; ...
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Different isomers of tetrachlorophenol exist according to which ring positions on the phenol contain chlorine atoms. There are three different isomers: 2,3,4,5-Tetrachlorophenol; 2,3,4,6-Tetrachlorophenol; 2,3,5,6-Tetrachlorophenol
There are six isomers: 2,3-Dichlorophenol; 2,4-Dichlorophenol; 2,5-Dichlorophenol; 2,6-Dichlorophenol; 3,4-Dichlorophenol; 3,5-Dichlorophenol; Dichlorophenols are used as intermediates in the manufacture of more complex chemical compounds, including the common herbicide 2,4-dichlorophenoxyacetic acid (2,4-D). [1]