Home Chemistry Heterocyclic Building Blocks Pyridines 3-Methoxypyridine
Electrophilic aromatic substitution: 3-Methoxypyridine can react with electrophiles such as acyl chlorides, acid anhydrides, or nitration reagents to substitute the methoxy group on the pyridine ring.
Nucleophilic substitution: The methoxy group in 3-methoxypyridine can be substituted by a nucleophile under suitable reaction conditions.
Oxidation: 3-Methoxypyridine can be oxidized to form pyridine N-oxide or other oxidation products under appropriate conditions.
Reduction: The pyridine ring or the methoxy group can be reduced to various products depending on the reagents and conditions used.
Alkylation/acylation: The nitrogen atom in the pyridine ring can undergo alkylation or acylation reactions with suitable alkylating or acylating agents.
Heterocyclic synthesis: 3-Methoxypyridine can participate in various heterocyclic synthesis reactions to form fused or spiro heterocyclic compounds.
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Lithium triisopropoxy(5-methoxypyridin-2-yl)borate
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4-Bromo-3-methoxypyridine hydrochloride
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4-(Chloromethyl)-3-methoxypyridine hydrochloride
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(3-Methoxypyridin-4-yl)methanamine hydrochloride
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