Home Chemistry Organic Building Blocks Bromides 4-Bromobenzo[C][1,2,5]Thiadiazole
Substitution Reactions: The bromine atom in 4-bromobenzo[c][1,2,5]thiadiazole can undergo nucleophilic substitution reactions. For example, it can be replaced by other nucleophiles (e.g., amino groups) to form substituted derivatives.
Electrophilic Aromatic Substitution: The benzene ring in the molecule can undergo electrophilic aromatic substitution reactions. This means that it can react with electrophilic reagents, such as strong acids or acylating agents, to introduce various functional groups onto the benzene ring.
Cross-Coupling Reactions: 4-bromobenzo[c][1,2,5]thiadiazole can be used as a substrate in palladium-catalyzed cross-coupling reactions, such as Suzuki, Stille, or Heck reactions, to form carbon-carbon or carbon-heteroatom bonds with other organic compounds.
Reductive Reactions: The compound can be subjected to reductive reactions, which may reduce functional groups and lead to the formation of saturated compounds.
Oxidation Reactions: 4-bromobenzo[c][1,2,5]thiadiazole can potentially undergo oxidation reactions, depending on the reaction conditions and reagents used.
Nucleophilic Addition Reactions: Depending on the substituents on the molecule, it can participate in nucleophilic addition reactions, where nucleophiles add to the molecule to form new compounds.
Formation of Polymers: This compound can be used as a monomer in polymerization reactions, such as Suzuki-Miyaura polymerization, to form conjugated polymers for various applications in materials science and electronics.
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4,7-Dibromo-5,6-bis(octyloxy)benzo[c][1,2,5]thiadiazole
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