4-(Trifluoromethyl)phenylboronic acid is commonly used as reagent for site-selective suzuki-miyaura cross-coupling reactions. It is also employed as building blocks in the preparation of thiazole derivatives for printable electronics and terphenyl benzimidazoles as tubulin polymerization inhibitors.
An Efficient Base-Free N-Arylation of Imidazoles and Amines with Arylboronic Acids Using Copper-Exchanged Fluorapatite. 
Efficient synthesis of arylated coumarins by site-selective Suzuki-Miyaura cross-coupling reactions of the bis(triflate) of 4-methyl-5,7-dihydroxycoumarin. 
Pd-catalyzed direct arylation of phenylpyrazole: Synthesis of fipronil derivatives with aryl boronic acids promoted by a stoichiometric amount of NIS. 
 M.Lakshmi Kantam, et al, J. Org. Chem., 2006, 71(25), pp 9522-9524.
 N.Eleya, et al, Synlett, 2012, 4(2), pp 223-226.
 X.H.Zhang, et al, J. F. Chem., 2012, 137, pp 44-49.
NONH for all modes of transport
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