Home Chemistry Heterocyclic Building Blocks Morpholines 4-(Pyridin-4-Yl)Morpholine
Substitution Reactions: The pyridine ring is susceptible to electrophilic aromatic substitution reactions, such as nitration, halogenation, or Friedel-Crafts acylation.
Nucleophilic Substitution: The morpholine ring may undergo nucleophilic substitution reactions at the nitrogen or carbon atoms. For example, you can perform nucleophilic substitution at the carbon with alkyl halides or other electrophiles, or at the nitrogen with various nucleophiles.
Alkylation or Acylation: You can alkylate or acylate the compound using appropriate alkyl or acyl halides to introduce new substituents on the morpholine or pyridine ring.
Oxidation and Reduction Reactions: Depending on the conditions and reagents used, you can oxidize or reduce functional groups within the molecule.
Ring Opening Reactions: The morpholine ring can be opened under specific reaction conditions, resulting in the formation of products with open-chain structures.
Metal-Catalyzed Reactions: Transition metal catalysts can be used to perform various transformations, including C-C bond formation reactions.
Cyclization Reactions: In some cases, the compound may undergo cyclization reactions to form structurally more complex molecules.
Hydrogenation: You can hydrogenate the pyridine or morpholine ring, depending on the catalyst and conditions used.
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