Product Information
Name:4-Bromopyridine hydrobromide
Brand:Biosynth
Description:The cross-coupling reaction of 4-bromopyridine hydrobromide is a powerful and efficient method for the synthesis of functionalized heterocycles. The sequence of this reaction is shown below:
The coupling reaction can be carried out in a one pot procedure with a variety of different functional groups. A wide range of products can be synthesized efficiently, including substituted pyridines, quinolines, indoles, imidazoles, and benzofurans. The Suzuki cross-coupling reaction is an example of a cross-coupling reaction that uses the boronic acid or boronate ester as the coupling partner. This type of coupling is typically more selective than other types due to its use of stoichiometric amounts of boronic acid or boronate ester. Another popular type of cross-coupling reaction that can be used with 4-bromopyridine hydrobromide
The coupling reaction can be carried out in a one pot procedure with a variety of different functional groups. A wide range of products can be synthesized efficiently, including substituted pyridines, quinolines, indoles, imidazoles, and benzofurans. The Suzuki cross-coupling reaction is an example of a cross-coupling reaction that uses the boronic acid or boronate ester as the coupling partner. This type of coupling is typically more selective than other types due to its use of stoichiometric amounts of boronic acid or boronate ester. Another popular type of cross-coupling reaction that can be used with 4-bromopyridine hydrobromide
Notice:Our products are intended for lab use only. For any other use, please contact us.
Chemical properties
Molecular weight:238.91 g/mol
Formula:C5H4BrN·HBr
Purity:Min. 95%