Home Chemistry Heterocyclic Building Blocks Quinoxalines 3,4-Dihydroquinoxalin-2(1H)-One
Substitution Reactions: Depending on the specific substitution reagents and conditions, the hydrogen atoms (H) can be replaced by various functional groups or substituents. For example, you can perform N-alkylation, N-acylation, or N-halogenation reactions.
Oxidation: The carbonyl group (C=O) in the compound can be oxidized to form a carboxylic acid or other oxidation products using appropriate oxidizing agents.
Reduction: The carbonyl group can be reduced to form the corresponding alcohol or other reduced products using reducing agents.
Cyclization Reactions: 3,4-dihydroquinoxalin-2(1H)-one can participate in various cyclization reactions to form cyclic compounds.
Condensation Reactions: It can undergo condensation reactions with other compounds to form new chemical products.
Base-Catalyzed Reactions: The compound can react with strong bases to undergo various transformations, such as deprotonation, rearrangement, or elimination reactions.
Hydrolysis: 3,4-dihydroquinoxalin-2(1H)-one can be hydrolyzed under appropriate conditions to form different products, depending on the reaction conditions.
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Ethyl 2-methyl-3-oxo-1,2,3,4-tetrahydroquinoxaline-6-carboxylate
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3,3-Dimethyl-3,4-dihydroquinoxalin-2(1H)-one
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4-Methyl-3,4-dihydroquinoxalin-2(1H)-one
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6-Chloro-1-methyl-3,4-dihydroquinoxalin-2(1H)-one
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