Home Chemistry Heterocyclic Building Blocks Imidazolidines Imidazolidine-2,4-Dione
Cyclization: Imidazolidine-2,4-dione can cyclize to form various derivatives. For example, it can react with primary amines to form hydantoin derivatives.
Ring-Opening Reactions: Imidazolidine-2,4-dione can undergo ring-opening reactions under certain conditions. For instance, it can react with strong bases to open the ring and form carboxylates.
Nucleophilic Addition Reactions: The carbonyl group in imidazolidine-2,4-dione is susceptible to nucleophilic attack. It can react with nucleophiles (e.g., amines or Grignard reagents) to form various products.
Oxidation: Imidazolidine-2,4-dione can undergo oxidation reactions to form hydantoin derivatives. For example, when exposed to mild oxidizing agents, it can be converted to N-substituted hydantoins.
Reduction: Imidazolidine-2,4-dione can also be reduced to form amines or other products by using reducing agents.
Halogenation: It can undergo halogenation reactions, where halogenating agents like chlorine or bromine can react with the imidazolidine-2,4-dione to introduce halogen atoms.
Condensation Reactions: Imidazolidine-2,4-dione can participate in condensation reactions to form various compounds, especially when reacting with other carbonyl compounds.
Substitution Reactions: Imidazolidine-2,4-dione can undergo substitution reactions, where functional groups can be replaced by other groups through various reaction mechanisms.
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Methyl 2-(2,5-dioxoimidazolidin-4-yl)acetate
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3-(4-Methyl-2,5-dioxoimidazolidin-4-yl)propanoic acid
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1,3-Bis(hydroxymethyl)-5,5-dimethylimidazolidine-2,4-dione
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1-Bromo-3-chloro-5,5-dimethylimidazolidine-2,4-dione
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