Chemistry Heterocyclic Building Blocks Benzimidazoles 1,2-Diphenyl-1H-Benzo[D]Imidazole

1,2-Diphenyl-1H-Benzo[D]Imidazole

Electrophilic Aromatic Substitution: The compound can undergo electrophilic aromatic substitution reactions, where electrophiles replace hydrogen atoms on the aromatic ring. For example, it can react with strong electrophiles like nitration (HNO3/H2SO4) or halogenation (e.g., bromination or chlorination) to introduce substituents on the aromatic ring. Nucleophilic Aromatic Substitution: It can also undergo nucleophilic aromatic substitution reactions, where nucleophiles can displace a leaving group on the aromatic ring. This typically occurs under specific conditions and with appropriate nucleophiles. Reduction: 1,2-diphenyl-1H-benzo[d]imidazole can be reduced using reducing agents like lithium aluminum hydride (LiAlH4) to produce the corresponding dihydro-1,2-diphenyl-1H-benzo[d]imidazole. Alkylation and Acylation: It can react with alkyl halides or acyl halides in the presence of a base to introduce alkyl or acyl groups onto the nitrogen atom or aromatic ring. Oxidation: Oxidation reactions can be employed to convert 1,2-diphenyl-1H-benzo[d]imidazole into other functionalized products. Condensation Reactions: It can participate in condensation reactions to form new chemical compounds. For example, it can react with aldehydes or ketones to form Schiff bases. Photophysical Reactions: Depending on the substitution pattern and the presence of specific functional groups, it may undergo photochemical reactions or photophysical processes.

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(1H-Benzo[D]Imidazol-2-Yl)Methanamine (1H-Benzo[D]Imidazol-2-Yl)Methanol 1,2-Diphenyl-1H-Benzo[D]Imidazole 1-Benzyl-1H-Benzo[D]Imidazole 1-Ethyl-1H-Benzo[D]Imidazole 1-Methyl-1H-Benzo[D]Imidazole 1-Phenyl-1H-Benzo[D]Imidazole 1H-Benzo[D]Imidazol-2-Amine 1H-Benzo[D]Imidazol-5-Amine 1H-Benzo[D]Imidazol-6-Amine 1H-Benzo[D]Imidazole-2-Carbaldehyde 1H-Benzo[D]Imidazole-2-Carboxylic Acid 1H-Benzo[D]Imidazole-2-Thiol 1H-Benzo[D]Imidazole-4-Carboxylic Acid 1H-Benzo[D]Imidazole-5-Carboxylic Acid 2-((Pyridin-2-Ylmethyl)Thio)-1H-Benzo[D]Imidazole 2-(1H-Benzo[D]Imidazol-2-Yl)Ethan-1-Amine 2-(Chloromethyl)-1H-Benzo[D]Imidazole 2-Benzyl-1H-Benzo[D]Imidazole 2-Bromo-1H-Benzo[D]Imidazole 2-Chloro-1H-Benzo[D]Imidazole 2-Methyl-1H-Benzo[D]Imidazole 4-Bromo-1H-Benzo[D]Imidazole 4-Methyl-1H-Benzo[D]Imidazole 5,6-Dichloro-1H-Benzo[D]Imidazole 5-Bromo-1H-Benzo[D]Imidazole 5-Chloro-1H-Benzo[D]Imidazole 5-Methoxy-1H-Benzo[D]Imidazole 5-Methyl-1H-Benzo[D]Imidazole 6-Chloro-1H-Benzo[D]Imidazole Methyl (1H-Benzo[D]Imidazol-2-Yl)Carbamate Methyl 1H-Benzo[D]Imidazole-2-Carboxylate Tert-Butyl 1H-Benzo[D]Imidazole-1-Carboxylate

By Key Group+−

Amino-Benzimidazole Benzimidazol-Amine Benzimidazole-Carboxylate Benzimidazole-Carboxylic Acid Benzimidazole-Carboxylic-Acid Benzimidazole-Hydrochloride Benzimidazole-Nitrile Benzoimidazol-Methanamine Benzoimidazol-Methanol Benzoimidazol-One Benzoimidazole-Thione Benzyl-Benzoimidazole Bromo-Benzimidazole Chloro-Benzimidazole Dimethyl-Benzoimidazole Dioxaborolane-Benzimidazole Fluoro-Benzoimidazole Hydroxy-Benzimidazole Methoxy-Benzoimidazole Methylbenzimidazole Nitro-Benzoimidazole Other-Benzimidazole Phenyl-Benzoimidazole Piperidine-Benzimidazole Pyridin-Benzoimidazole Trifluoromethyl-Benzimidazole

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Aromatic Heterocycles Other Aliphatic Heterocycles Oxadiazoles Piperazines Piperidines Pyridines Pyrimidines Pyrroles Tetrahydropyrans Thiophenols

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Alcohols Aldehydes Alkenyls Amides Amines Aryls Bromides Carboxylic Acids Chiral Building Blocks Chlorides Difluoromethyls Esters Ethers Fluorinated Building Blocks Hydrazines Iodides Nitriles Nitroes Phenols Sulfamides Sulfides Sulfonic Acids Sulfoxides Trifluoromethyls

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