15776-99-5

Basic information

• Product Name: 1-benzyl-5,6-dimethyl-1H-benzo[d]imidazole
• Synonyms: 1-benzyl-5,6-dimethyl-1H-benzo[d]imidazole
• CAS NO: 15776-99-5
• Molecular Weight: 236.316
• Mol File: 15776-99-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-benzyl-5,6-dimethyl-1H-benzo[d]imidazole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-benzyl-5,6-dimethyl-1H-benzo[d]imidazole(15776-99-5)
• EPA Substance Registry System: 1-benzyl-5,6-dimethyl-1H-benzo[d]imidazole(15776-99-5)

Safety Data

• Hazardous Substances Data: 15776-99-5(Hazardous Substances Data)

Upstream product

• 582-60-5 5,6-dimethyl-1H-benzo[d]imida-zole 
• 100-44-7 benzyl chloride 
• 100-39-0 benzyl bromide 

Downstream Products

• 1250258-07-1 (Z)-2-{9-benzyl-2,2,6,7-tetramethyl-9,9a-dihydro[1,3]oxazolo[3,2-a]benzimidazol-3(2H)-yliden}acetonitrile 
• 582-60-5 5,6-dimethyl-1H-benzo[d]imida-zole 

Relevant articles and documents

Selective C-H trifluoromethylation of benzimidazoles through photoredox catalysis

The protocol presented here is a new strategy for visible light induced C-H trifluoromethylation at C4 of benzimidazoles using Togni's reagent in the presence of fac-Ir(ppy)3. Its advantages are its operational simplicity, mild reaction conditions, low catalyst loading and wide substrate scope in which electron-withdrawing, electron-donating groups and different protecting groups are tolerated.

Cu-Catalyzed Regioselective C-H Alkylation of Benzimidazoles with Aromatic Alkenes

Herein we report a novel Cu-catalyzed regioselective C2-H alkylation of benzimidazoles with aromatic alkenes. The reaction features exclusive regioselectivity and broad substrate scope in the intermolecular alkylation of benzimidazoles with terminal and i

SYNTHESIS OF ONCOLYTIC ANALOGS OF 1,2-DIMETHYL-4,5-DIAMINOBENZENE.

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