Home Chemistry Heterocyclic Building Blocks Thiadiazoles Benzo[D][1,2,3]Thiadiazole
Electrophilic Aromatic Substitution (EAS): Benzo[d][1,2,3]thiadiazole can undergo EAS reactions, such as nitration, halogenation, and sulfonation, at its aromatic ring.
Nucleophilic Substitution: The nitrogen and sulfur atoms in the thiadiazole ring can serve as sites for nucleophilic substitution reactions. For example, they can be alkylated, acylated, or undergo other substitution reactions.
Reductive Processes: Benzo[d][1,2,3]thiadiazole can undergo reduction reactions, such as hydrogenation or metal-catalyzed reductions, to yield various derivatives.
Oxidation: The compound can be oxidized to produce derivatives with different functional groups.
Coupling Reactions: Benzo[d][1,2,3]thiadiazole can participate in coupling reactions, like Suzuki-Miyaura coupling or Heck coupling, to form more complex molecules.
Condensation Reactions: Benzo[d][1,2,3]thiadiazole can be used in condensation reactions to create larger molecules, such as polymers or dendrimers.
Metal-Catalyzed Reactions: It can serve as a ligand in metal-catalyzed reactions, forming coordination complexes with various transition metals.
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Benzo[d][1,2,3]thiadiazole-5-carbaldehyde
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