Home Chemistry Heterocyclic Building Blocks Piperazines Piperazine-2,5-Dione
Hydrolysis: Piperazine-2,5-dione can undergo hydrolysis in the presence of an acid or base to yield piperazine and carbon dioxide.
Reduction: Piperazine-2,5-dione can be reduced to piperazine-2,5-diamine using reducing agents such as sodium borohydride or hydrogen gas in the presence of a catalyst.
Alkylation and Acylation: The nitrogen atoms in the piperazine ring can undergo alkylation or acylation reactions to introduce various substituents, resulting in the formation of new compounds.
Ring Opening: Piperazine-2,5-dione can undergo ring-opening reactions under specific conditions, leading to the formation of open-chain compounds.
Condensation Reactions: It can participate in condensation reactions with other compounds, leading to the formation of various heterocyclic compounds.
Oxidation: Piperazine-2,5-dione can undergo oxidation reactions under appropriate conditions, resulting in the formation of oxidized products.
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cis-3,6-Bis(2-hydroxyethyl)piperazine-2,5-dione
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(3S,6S)-3,6-Diisopropylpiperazine-2,5-dione
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