Abstract
4,4′-Dichloro-3,5,3′,5′-tetramethylbiphenyl was prepared by bis -diazotization of 3,5,3′,5′-tetramethylbenzidine followed by the Sandmeyer reaction. The starting material is a noncarcinogenic analogue of benzidine, and the product may be of interest as a model compound for studying the metabolism of chlorinated biphenyls.
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