1434057-17-6

Basic information

• Product Name: 1-(4-bromophenyl)-3-phenyl-1H-imidazol-3-ium tetrafluoroborate
• Synonyms: 1-(4-bromophenyl)-3-phenyl-1H-imidazol-3-ium tetrafluoroborate
• CAS NO: 1434057-17-6
• Molecular Weight: 386.982
• Mol File: 1434057-17-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-(4-bromophenyl)-3-phenyl-1H-imidazol-3-ium tetrafluoroborate(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-bromophenyl)-3-phenyl-1H-imidazol-3-ium tetrafluoroborate(1434057-17-6)
• EPA Substance Registry System: 1-(4-bromophenyl)-3-phenyl-1H-imidazol-3-ium tetrafluoroborate(1434057-17-6)

Safety Data

• Hazardous Substances Data: 1434057-17-6(Hazardous Substances Data)

Upstream product

• 10040-96-7 1-(4-bromophenyl)-1H-imidazole 
• 7164-98-9 1-phenylimidazole 
• 5467-74-3 4-Bromophenylboronic acid 
• 106-37-6 1.4-dibromobenzene 

Relevant articles and documents

Heterogeneous sequential N-arylation of N-heterocycles over copper anchored mesoporous silica catalyst

N-Arylation reaction of N-heterocyclic compounds has been carried out in excellent yield using copper anchored SBA-15 catalyst. Sequential N-arylation reactions employing single catalyst under heterogeneous condition provides a straightforward access to a

Copper-catalyzed direct aryl quaternization of N-substituted imidazoles to form imidazolium salts

Diaryliodonium salts are employed to directly quaternize N-substituted imidazoles by using a copper catalyst to construct aryl imidazolium salts in moderate to excellent yields. This transformation is tolerant to a broad range of functional groups and provides a straightforward, efficient, and versatile route to synthesize aryl imidazolium as well as triazolium salts, especially the unsymmetric version.