Home Chemistry Heterocyclic building blocks Pyridines 3,5-dimethylpyridine
Nucleophilic substitution: The nitrogen atom in the pyridine ring can undergo nucleophilic substitution reactions with electrophiles. This can lead to the formation of substituted products.
Acylation: 3,5-dimethylpyridine can react with acyl chlorides or acid anhydrides to form N-acyl derivatives. This is a common reaction for compounds containing nitrogen atoms.
Alkylation: It can react with alkyl halides or alkylating agents under appropriate conditions to give N-alkylated products.
Oxidation: Collidine can be oxidized to produce various oxidation products, depending on the oxidizing agent used and reaction conditions.
Condensation reactions: It can participate in condensation reactions, particularly with carbonyl compounds, leading to the formation of imines or related compounds.
Protonation: The nitrogen atom in the pyridine ring can undergo protonation reactions under acidic conditions.
Reduction: Collidine can be reduced to form tetrahydropyridine derivatives under appropriate conditions.
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(4-Methoxy-3,5-dimethylpyridin-2-yl)methyl acetate
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4-Bromo-3,5-dimethylpyridine hydrochloride
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