Home Chemistry Heterocyclic Building Blocks Carbazole Series 7H-Benzo[C]Carbazole
Electrophilic aromatic substitution: This compound can undergo electrophilic aromatic substitution reactions where electrophiles (electron-deficient species) replace hydrogen atoms on the benzene rings. Common electrophiles include nitration, halogenation, and Friedel-Crafts acylation or alkylation.
Reduction: 7H-benzo[c]carbazole can be reduced to its dihydro derivative by catalytic hydrogenation, using hydrogen gas and a suitable catalyst like palladium on carbon.
Oxidation: Oxidation reactions can be performed to convert 7H-benzo[c]carbazole into various functionalized products. Common oxidizing agents like potassium permanganate or chromic acid can be used.
Substitution reactions: You can introduce various functional groups at different positions on the molecule through nucleophilic aromatic substitution reactions. This could include reactions with amines, alkoxides, and other nucleophiles.
Diels-Alder reaction: 7H-benzo[c]carbazole can participate in Diels-Alder reactions, where it acts as a diene or dienophile, forming cyclic compounds with suitable dienophiles.
Suzuki-Miyaura coupling: This compound can be used in Suzuki-Miyaura coupling reactions to form biaryl compounds when reacting with suitable aryl halides or boronic acids.
Ring-opening reactions: 7H-benzo[c]carbazole can undergo ring-opening reactions, leading to the formation of open-chain structures under appropriate conditions.
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