Chemistry Heterocyclic Building Blocks Triazoles 4-phenyl-4H-1,2,4-triazole
Acylation: You can acylate the nitrogen atoms in the triazole ring using acylating agents, forming amide derivatives.
Alkylation: Alkylating agents can be used to add alkyl groups to the nitrogen atoms in the triazole ring.
Reduction: Reduction reactions can be performed to reduce the nitrogen atoms in the triazole ring, typically by using reducing agents.
Oxidation: Oxidation reactions can be performed on the compound to convert it into other functional groups.
Hydrogenation: You can hydrogenate the compound to saturate the aromatic ring and convert it into a saturated derivative.
Halogenation: You can perform halogenation reactions by introducing halogen atoms (e.g., Cl, Br) to the aromatic ring of the triazole.
Condensation Reactions: 4-phenyl-4H-1,2,4-triazole can participate in condensation reactions with other compounds, forming new chemical products.
Metal-Catalyzed Reactions: Transition metal-catalyzed reactions, such as Suzuki-Miyaura coupling or Buchwald-Hartwig amination, can be used to modify the structure of 4-phenyl-4H-1,2,4-triazole.
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N-(3-(4H-1,2,4-Triazol-4-yl)phenyl)acetamide
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2-(4-(4H-1,2,4-Triazol-4-yl)phenyl)acetic acid