Home Chemistry Heterocyclic Building Blocks Imidazoles 2-Phenyl-1H-Benzo[D]Imidazole
Acylation: You can acylate the imidazole nitrogen with an acyl chloride or anhydride to introduce an acyl group to the nitrogen atom.
Alkylation: The imidazole nitrogen can also be alkylated using alkyl halides or alkyl sulfonates.
Amination: You can introduce amino groups to the molecule through nucleophilic substitution reactions.
Hydrogenation: The phenyl ring can be reduced to a cyclohexyl ring using a suitable reducing agent.
Oxidation: The phenyl ring can be oxidized to a benzoic acid or other oxidized derivatives.
Substitution Reactions: The phenyl ring can undergo electrophilic aromatic substitution reactions, such as nitration, halogenation, or sulfonation.
Nucleophilic Addition: If there are suitable functional groups, nucleophilic addition reactions can occur on the imidazole ring or phenyl ring.
Reduction: Depending on the reaction conditions, you can reduce various functional groups in the molecule.
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4-(6-Chloro-1H-benzo[d]imidazol-2-yl)phenol
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2-(1H-Benzo[d]imidazol-2-yl)-4-bromophenol
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4-(5,7-Dichloro-1H-benzo[d]imidazol-2-yl)aniline
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4-(5-Chloro-1H-benzo[d]imidazol-2-yl)aniline
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2-(4-(Dimethylamino)phenyl)-1H-benzo[d]imidazol-5-amine
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2-(3-Aminophenyl)-1H-benzo[d]imidazol-6-amine
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