Home Chemistry Heterocyclic Building Blocks Pyridines 2-Bromo-3-Fluoropyridine
Nucleophilic substitution: The bromine atom is often reactive towards substitution reactions, where it can be replaced by other nucleophiles such as amines, thiols, or organometallic reagents.
Electrophilic substitution: The fluorine atom can act as a directing group in electrophilic aromatic substitution reactions, where a new substituent is introduced onto the pyridine ring.
Metalation: The bromine atom can be removed under suitable conditions, leading to the formation of a pyridine derivative that has a metal atom attached at the position originally occupied by bromine.
Cross-coupling reactions: Both bromine and fluorine atoms can participate in cross-coupling reactions with appropriate partners, leading to the formation of biaryl or heteroaryl compounds.
Redox reactions: The presence of both bromine and fluorine atoms can make the compound susceptible to various redox reactions, including oxidation or reduction of the functional groups.
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2-Bromo-3-fluoro-6-(trifluoromethyl)pyridine
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