Home Chemistry Heterocyclic Building Blocks Pyridines 2-Bromo-5-(Trifluoromethyl)Pyridine
Nucleophilic substitution reactions: The bromine atom can be replaced by a nucleophile such as amines, alkoxides, or thiols.
Cross-coupling reactions: The bromine atom can undergo coupling reactions with various nucleophiles or electrophiles in the presence of transition metal catalysts.
Palladium-catalyzed reactions: palladium catalysts can promote various transformations such as Suzuki, Heck, Sonogashira, or Stille reactions.
Fluorination reactions: The trifluoromethyl group may undergo fluorination reactions under suitable conditions.
Functional group transformations: The bromine and trifluoromethyl groups can participate in a variety of transformations, including oxidation, reduction, and substitution reactions.
Ring-closure reactions: The pyridine ring can undergo various ring-closure reactions to form heterocyclic compounds.
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2-Bromo-5-(trifluoromethyl)pyridin-3-amine
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Methyl 6-bromo-3-(trifluoromethyl)picolinate
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2-Bromo-5-(trifluoromethyl)isonicotinic acid
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2-Bromo-3-nitro-5-(trifluoromethyl)pyridine
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2-Bromo-3-methoxy-5-(trifluoromethyl)pyridine
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