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Preferred IUPAC name. 2,3-Dichlorophenol. Identifiers ... 2,3-Dichlorophenol (2,3-DCP) is a chlorinated derivative of phenol with the molecular formula Cl 2 C 6 H 3 OH.
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 ]
3,4-Dichlorophenol Names Preferred IUPAC name. ... (3,4-DCP) is a chlorinated derivative of phenol with the molecular formula Cl 2 C 6 H 3 OH. References
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
2,6-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]
2,4-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).
3,4-DCPP, CAS# 57260-67-0. The positional isomer 3,4-dichlorophenylpiperazine (3,4-DCPP) is also known, and acts as both a serotonin releaser via the serotonin transporter, [8] and a β 1-adrenergic receptor blocker, [9] though with relatively low affinity at both targets.
2,3-Dichlorobutadiene is a chlorinated derivative of butadiene. This colorless liquid is prone to polymerization, more so than 2-chlorobutadiene. It is used to produce specialized neoprene rubbers. It can be prepared by the copper-catalyzed isomerization of dichlorobutynes. Alternatively dehydrochlorination of 2,3,4-trichloro-1-butene: [1]