Home Chemistry Heterocyclic Building Blocks Pyridines Ethyl Isonicotinate
Nucleophilic Substitution: Ethyl ethyl isonicotinate can undergo nucleophilic substitution reactions where a nucleophile replaces one of the substituents on the molecule. This can lead to the formation of various products depending on the nature of the nucleophile and reaction conditions.
Acylation: Ethyl ethyl isonicotinate can undergo acylation reactions, where an acyl group is introduced onto the molecule. This can occur through reactions with acyl halides, acid anhydrides, or acyl chlorides.
Reduction: Ethyl ethyl isonicotinate can be reduced to produce different compounds, such as ethyl isonicotinate or related derivatives. Reduction reactions can be achieved using various reducing agents, such as metal hydrides (e.g., lithium aluminum hydride) or catalytic hydrogenation.
Cyclization: Ethyl ethyl isonicotinate can participate in cyclization reactions, forming cyclic compounds through intramolecular reactions. This can lead to the formation of heterocycles or carbocycles depending on the reaction conditions and the structure of the molecule.
Condensation: Ethyl ethyl isonicotinate can undergo condensation reactions with other compounds, leading to the formation of new bonds and larger molecules. Condensation reactions can occur through a variety of mechanisms, such as aldol condensation or Claisen condensation.
Oxidation: Ethyl ethyl isonicotinate can be oxidized to produce various oxidation products. Oxidation reactions can be achieved using oxidizing agents such as potassium permanganate, chromium trioxide, or peracids.
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Ethyl 5-bromo-2-(trifluoromethyl)isonicotinate
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