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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 ]
2,6-Dichlorophenol is a compound with formula C 6 H 3 Cl 2 OH. It is one of the six isomers of dichlorophenol. It is a colorless solid. Its pK a is 6.78, which is about 100x more acidic than 2-chlorophenol (8.52) and 1000x more acidic than phenol itself (9.95). [3]
2,3-Dichlorophenol (2,3-DCP) is a chlorinated derivative of phenol with the molecular formula Cl 2 C 6 H 3 OH. References. Cited sources Haynes, William M., ed. (2016
Dichlorophen is an anticestodal agent, fungicide, germicide, and antimicrobial agent. [2] It is used in combination with toluene for the removal of parasites such as ascarids, hookworms, and tapeworms from dogs and cats. [3]
The 2,6 and 3,5 isomers do not form acceptably from toluene or chlorotoluenes, so these isomers are prepared by indirect methods. For example, 2,6-dichlorotoluene can be prepared by chlorination of 4-toluenesulfonyl chloride followed by desulfonation .
January 3, 2025 at 8:32 AM. WASHINGTON (Reuters) - -Alcoholic drinks should carry a label warning consumers about their cancer risks, the U.S. Surgeon General said in an advisory on Friday, noting ...
(The Center Square) – Texas has filed a lawsuit against several large chemical companies alleging they manufacture toxic forever chemicals used in products marketed as safe for families. Texas ...
[3] (C 6 H 5 ) 2 CCl 2 + H 2 O → (C 6 H 5 ) 2 CO + 2 HCl It is used in the synthesis of tetraphenylethylene , [ 5 ] diphenylmethane imine hydrochloride and benzoic anhydride .