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Sigma Aldrich Phenylmagnesium Bromide Solution
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Description
Phenylmagnesium bromide solution contains 3M phenylmagnesium bromide in diethyl ether. It can act as a strong acid and Lewis acid. It can undergo addition reaction with many unsaturated functional groups. The phenyl group can displace halide from other organic compounds. Phenylmagnesium bromide is a Grignard reagent. Reaction of +a-cyclohexanedione (dihydroresorcinol) with phenylmagnesium bromide has been investigated.Phenylmagnesium bromide was used for the synthesis of end-functionalized regioregular poly(3-alkylthiophene)s. It was also used for the monoalkylation of aliphatic primary amine to generate secondary amines by the Grignard reaction of 1-[(alkylamino) methyl] benzotriazoles. It may be used for synthesis of the following: 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 benzophenonesStorage below 25°C may cause formation of crystalline magnesium salts. Moving container to a war mLocation and occasional gentle swirling should redissolve the solid
Specifications
Specifications
| CAS | 100-58-3 |
| Density | 1.134 g/mL at 25°C |
| Molecular Formula | C6H5BrMg |
| Linear Formula | C6H5MgBr |
| MDL Number | MFCD00000038 |
| Quantity | 800 mL |
| Molecular Weight (g/mol) | 181.31 g/mol |
| Biological Activity | Central Nervous System |
Product Title
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