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1,3,5-Trichlorobenzene is an organochlorine compound. It is one of the three isomers of trichlorobenzene. Being more symmetrical than the other isomers, it exists as colourless crystals whereas the other isomers are liquids at room temperature. It is not formed upon chlorination of benzene.
Trichlorobenzene (TCB) may refer to any of three isomeric chlorinated derivatives of benzene with the molecular formula C 6 H 3 Cl 3. They differ by the positions of the chlorine atoms around the ring:
1,2,3-Trichlorobenzene is an organochlorine compound with the chemical formula C 6 H 3 Cl 3. [ 1 ] [ 2 ] This is one of three isomers of trichlorobenzene ; the two others are 1,2,4-Trichlorobenzene and 1,3,5-Trichlorobenzene .
The LD50 (oral, rats) is 756 mg/kg. Animal studies have shown that 1,2,4-trichlorobenzene affects the liver and kidney, and is possibly a teratogen. [4] There is no regulated occupational exposure limit for chemical exposure, but the National Institute for Occupational Safety and Health recommends no greater exposure than 5 ppm, over an 8-hour workday.
The 2,4,6- isomer is easily produced by deprotonation of 1,3,5-trichlorobenzene followed by reaction with carbon dioxide. [1] Its conversion to 2,4,6-trichlorobenzoyl chloride makes it a key intermediate in the Yamaguchi esterification protocol.
Chlorobenzenes are a group of aryl chlorides/halobenzenes consisting of one or more chlorine atoms as substituents on a benzene core. They have the formula C 6 H 6–n Cl n, where n = 1–6 is the number of chlorine atoms.
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Name CAS Number InChIKey Descriptors 0 C 12 H 10: Biphenyl 92-52-4 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 1 C 12 H 9 Cl: 2-Chlorobiphenyl 2051-60-7 LAXBNTIAOJWAOP-UHFFFAOYSA-N CP1 2 C 12 H 9 Cl: 3-Chlorobiphenyl 2051-61-8 NMWSKOLWZZWHPL-UHFFFAOYSA-N CP0 3 C 12 H 9 Cl: 4-Chlorobiphenyl 2051-62-9 FPWNLURCHDRMHC-UHFFFAOYSA-N CP0 4 C 12 H 8 Cl 2: 2,2 ...