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The batch implicated in these deaths also contained vital synthesis impurities, which may have contributed to the toxicity. The primary synthesis of racemic Bromo-DragonFLY was reported by David E. Nichols in 1998 and was an expansion upon earlier research into the tetrahydrobenzodifuran analogue of DOB. The 1998 synthesis of racemic Bromo-DragonFLY starts from hydroquinone, which is dialkylated with 1-bromo-2-chloroethane, brominated, and וילות להשכרה יומית treated with n-butyllithium to yield the tetrahydrobenzodifuran ring system. A Cooperative Intelligent Transport System (C-ITS). After para-bromination and oxidation of the ring system with DDQ, the amine was deprotected yielding (R)-(-)-Bromo-DragonFLY. The 2001 enantiospecific synthesis of (R)-(-)-Bromo-DragonFLY by Nichols et al. Parker MA, Marona-Lewicka D, Lucaites VL, Nelson DL, Nichols DE (December 1998). “A novel (benzodifuranyl)aminoalkane with extremely potent exercise at the 5-HT2A receptor”. Parker, Matthew; Marona-Lewicka, צימר בצפון Danuta; Lucaites, Virginia; Nelson, David; Nichols, David (8 June 1998). “A Novel (Benzodifuranyl)aminoalkane with Extremely Potent Activity at the 5-HT2A Receptor”. For 2012, former Roush Fenway Racing driver David Ragan drove the automobile full-time. As of 12 March 2012, Bromo-DragonFLY is an unlawful designer drug.

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