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Phenyl magnesium bromide is the suitable reagent used for the synthesis of end-functionalized regioregular poly(3-alkylthiophene)s. It may be used for synthesis of 1,3,3-trimethyl-6-phenyl-2-oxabicyclo[2.2.2]octan-6-ol, 6-benzyl-1,3,3-trimethyl-2-oxabicyclo[2.2.2]octan-6-ol, (3-(2-Dithiobenzoatepropionyl)propyl)dimethylmethoxysilane, reversible addition-fragmentation chain transfer polymerization (RAFT)-silane agent, series of o-substituted benzophenones.
W. H. Urry.; M. S. Kharasch. Factors Influencing the Course and Mechanism of Grignard Reactions. XV. The Reaction of β,β-Dimethylphenethyl Chloride with Phenylmagnesium Bromide in the Presence of Cobaltous Chloride. J. Am. Chem. Soc. 1944, 66 (9),1438-1440.
G. Stucky.; R. E. Rundle. The Constitution of the Grignard Reagent, Phenylmagnesium Bromide Dietherate. J. Am. Chem. Soc. 1964, 87 (22),4825-4830.
Gefahrenhinweise (EU): H225-H314-H318
Highly flammable liquid and vapour. Causes severe skin burns and eye damage. Causes serious eye damage.
Keep away from heat/sparks/open flames/hot surfaces. - No smoking. IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.