1,3,5-Trichlorobenzene

477204689 1,3,5-Trichlorobenzene.svg 150px skin-invert Sample of 1,3,5-trichlorobenzene.jpg 1,3,5-Trichlorobenzene sym-Trichlorobenzene correct CAS 108-70-3 1635233 correct chemspider 7662 correct EBI 49916 correct EBI 44228 203-608-6 601358 7950 correct drugbank DB03836 1/C6H3Cl3/c7-4-1-5(8)3-6(9)2-4/h1-3H DC2100100 correct kegg correct FDA 2HS4M0BX3C Clc1cc(Cl)cc(Cl)c1 XKEFYDZQGKAQCN-UHFFFAOYAQ correct chemspider 1S/C6H3Cl3/c7-4-1-5(8)3-6(9)2-4/h1-3H correct chemspider XKEFYDZQGKAQCN-UHFFFAOYSA-N 1,3,5-Trichlorobenzene, International Programme on Chemical Safety 6 3 3 White solid 63 208.0 Jaw Ching-Guang Chen I-Ming Yen Jui-Hung Wang Yei-Shung December 1999 Partial solubility parameters of chlorobenzene and chlorophenol compounds at equilibrium distribution in two immiscible phases Chemosphere 39 15 2607–2620 10.1016/s0045-6535(99)00173-3 1999Chmsp..39.2607J 0045-6535 0.6 mg/100 mL MSDS for 1,3,5-Trichlorobenzene 107 800 mg/kg (oral, rat)3350 mg/kg (oral, mouse) 07 Warning 302 312 315 319 332 335 412 261 264 270 271 273 280 301+312 302+352 304+312 304+340 305+351+338 312 321 322 330 332+313 337+313 362 363 403+233 405 501 1,2,3-Trichlorobenzene1,2,4-Trichlorobenzene1,3,5-Tribromobenzene 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. Instead it is prepared by the Sandmeyer reaction from 3,5-dichloroaniline.U. Beck E. Löser Chlorinated Benzenes and Other Nucleus-Chlorinated Aromatic Hydrocarbons Ullmann's Encyclopedia of Industrial Chemistry 2012 Wiley-VCH Weinheim 10.1002/14356007.o06_o03 978-3527306732 See also Chlorobenzenes—different numbers of chlorine substituents and isomeric forms References Category:Chlorobenzenes