Home Chemistry Heterocyclic Building Blocks Pyridines 2-Chloro-3-(Trifluoromethyl)Pyridine
Nucleophilic substitution: The chlorine atom can be replaced by a nucleophile, such as amines, alcohols, or thiols, to yield various substituted derivatives.
Electrophilic aromatic substitution: The electron-rich pyridine ring can undergo electrophilic aromatic substitution reactions with electrophiles such as acyl chlorides, alkyl halides, or nitro compounds.
Metalation: The hydrogen atom on the pyridine ring can be replaced by a metal, such as lithium or magnesium, to form organometallic intermediates.
Cross-coupling reactions: The trifluoromethyl group can undergo cross-coupling reactions with suitable partners, such as aryl or vinyl halides, in the presence of transition metal catalysts.
Oxidation and reduction: The compound can be oxidized or reduced at various positions, leading to the formation of different functional groups.
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6-Chloro-5-(trifluoromethyl)pyridin-3-ol
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2-Chloro-5-nitro-3-(trifluoromethyl)pyridine
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2-Chloro-3,5-bis(trifluoromethyl)pyridine
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Methyl 6-chloro-5-(trifluoromethyl)nicotinate
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6-Chloro-5-(trifluoromethyl)pyridine-3-sulfonamide
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6-Chloro-5-(trifluoromethyl)pyridin-3-amine
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6-Chloro-5-(trifluoromethyl)nicotinaldehyde
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(6-Chloro-5-(trifluoromethyl)pyridin-3-yl)methanol
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(6-Chloro-5-(trifluoromethyl)pyridin-3-yl)methanamine
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(6-Chloro-5-(trifluoromethyl)pyridin-3-yl)boronic acid
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6-Chloro-5-(trifluoromethyl)nicotinic acid
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