Home Chemistry Heterocyclic Building Blocks Carbazole Series 9-Benzyl-9H-Carbazole
Friedel-Crafts Acylation: You can acylate the carbazole ring by using acylating agents such as acyl chlorides or anhydrides in the presence of Lewis acids like aluminum chloride.
Friedel-Crafts Alkylation: It can also undergo alkylation with alkyl halides or toluene in the presence of Lewis acids like aluminum chloride.
Suzuki Coupling: It can participate in Suzuki cross-coupling reactions, which involve the coupling of aryl halides with boronic acids in the presence of a palladium catalyst.
Bromination or Chlorination: The benzyl group can be brominated or chlorinated using the appropriate halogenating agents.
Hydrogenation: The aromatic ring can be hydrogenated to yield a saturated ring in the presence of a suitable catalyst such as palladium on carbon.
Oxidation: The compound can be oxidized using various oxidizing agents to introduce oxygen-containing functional groups.
Reduction: The carbonyl group in the benzyl moiety can be reduced to an alcohol using reducing agents like sodium borohydride or lithium aluminum hydride.
Grignard Reaction: You can form a Grignard reagent from the benzyl halide and react it with various electrophiles.
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9-Benzyl-9H-carbazole-3,6-dicarbaldehyde
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