Home Chemistry Heterocyclic Building Blocks Pyridines 3-Bromo-5-Methylpyridine
Nucleophilic substitution reactions: The bromine atom in the molecule can be substituted by various nucleophiles such as amines, thiols, or cyanide ions to yield corresponding substituted products.
Metalation reactions: The pyridine ring can undergo metalation reactions with strong bases to form metal complexes, which can then participate in further reactions or catalytic processes.
Cross-coupling reactions: 3-bromo-5-methylpyridine can undergo cross-coupling reactions, such as Suzuki-Miyaura coupling or Heck reaction, to form biaryl or alkylated products, respectively.
Redox reactions: The bromine atom can participate in redox reactions, either as an oxidizing or reducing agent, depending on the reaction conditions and the nature of the reactants involved.
Functional group transformations: The methyl group and the bromine atom can undergo various functional group transformations such as oxidation, reduction, or substitution reactions to yield diverse products with altered functional groups.
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tert-Butyl (5-bromo-3-methylpyridin-2-yl)carbamate
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1-(5-Bromo-3-methylpyridin-2-yl)-2,2,2-trifluoroethan-1-one
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1-(5-Bromo-3-methylpyridin-2-yl)ethanone
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