1384979-73-0

Basic information

• Product Name: N,N'-bis-(2,4,6-tri(1-butyl)phenyl)-4,5-dihydroimidazolium chloride
• Synonyms: N,N'-bis-(2,4,6-tri(1-butyl)phenyl)-4,5-dihydroimidazolium chloride
• CAS NO: 1384979-73-0
• Molecular Weight: 595.396
• Mol File: 1384979-73-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N,N'-bis-(2,4,6-tri(1-butyl)phenyl)-4,5-dihydroimidazolium chloride(CAS DataBase Reference)
• NIST Chemistry Reference: N,N'-bis-(2,4,6-tri(1-butyl)phenyl)-4,5-dihydroimidazolium chloride(1384979-73-0)
• EPA Substance Registry System: N,N'-bis-(2,4,6-tri(1-butyl)phenyl)-4,5-dihydroimidazolium chloride(1384979-73-0)

Safety Data

• Hazardous Substances Data: 1384979-73-0(Hazardous Substances Data)

Upstream product

• 841-07-6 1,3,5-tributylbenzene 
• 1384979-71-8 N,N'-bis-(2,4,6-tri(1-butyl)phenyl)ethylenediamine 
• 122-51-0 orthoformic acid triethyl ester 

Relevant articles and documents

General and highly efficient fluorinated-N-heterocyclic carbene-based catalysts for the palladium-catalyzed Suzuki-Miyaura reaction

A general and highly efficient trifluoromethylated-N-heterocyclic carbene (NHC)-based catalyst for the palladium-catalyzed Suzuki-Miyaura reaction was reported. In the presence of the catalyst, reactions of non-activated aryl chlorides and triflates with aryl boronic acids occurred at room temperature with good to excellent yields (63-98%). In addition, catalysts generated from a combination of Pd(OAc)2/imidazolium salt 6a is not only effective for the coupling of heteroaryl boronic acid with aryl halides and heteroaryl halides, but also efficient for coupling of other heteroaryl halides and heteroaryl boronic acids. Finally, the catalyst is highly effective for Suzuki-Miyaura reaction of aryl bromides and chlorides with 0.01-0.1 mol % loading if the temperature was raised at refluxed THF/H2O.