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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 ]
2,4,6-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
Download as PDF; Printable version; In other projects ... 2,5-Dichlorophenol Names Preferred IUPAC name. 2,5-Dichlorophenol ... is a chlorinated derivative of phenol ...
Download as PDF; Printable version; In other projects ... 3,4-Dichlorophenol Names Preferred IUPAC name. 3,4-Dichlorophenol ... with the molecular formula Cl 2 C 6 H ...
Name CAS number CH 3 CHO: acetaldehyde: 75-07-0 CH 3 CO 2 H: acetic acid: 64-19-7 (CH 3) 2 CO: acetone: 67-64-1 CH 3 CN: acetonitrile: 75-05-8 CH 3 CH 2 CH(OH)CH 2 OH: 1,2-Butanediol: 584-03-2 CH 3 CH(OH)CH 2 CH 2 OH: 1,3-Butanediol: 107-88-0 HOCH 2 CH 2 CH 2 CH 2 OH: 1,4-Butanediol: 110-63-4 C 6 H 14 O 2: 2-Butoxyethanol: 111-76-2 CH 3 CH 2 CH ...
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]
Dichloroanilines are chemical compounds which consist of an aniline ring substituted with two chlorine atoms and have the molecular formula C 6 H 5 Cl 2 N. There are six isomers, varying in the positions of the chlorine atoms around the ring relative to the amino group. As aniline derivatives, they are named with the amino group in position 1.