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2,5-Dichlorophenol (2,5-DCP) is a ... Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply. By using this site, ...
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 ]
2,4-Dichlorophenol (2,4-DCP) is a chlorinated derivative of phenol with the molecular formula Cl 2 C 6 H 3 OH. It is a white solid that is mildly acidic (pK a = 7.9). It is produced on a large scale as a precursor to the herbicide 2,4-dichlorophenoxyacetic acid (2,4-D).
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.
2,6-Dichlorophenol; 3,5-Dichlorophenol; 3,4-Dichlorophenol; ... Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; ...
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 .
The 4 substrates of this enzyme are 2,4-dichlorophenol, NADPH, H +, and O 2, whereas its 3 products are 3,5-dichlorocatechol, NADP +, and H 2 O. This enzyme belongs to the family of oxidoreductases , specifically those acting on paired donors, with O2 as oxidant and incorporation or reduction of oxygen.
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]