1175017-41-0

Basic information

• Product Name: (CH₃)5C₆CH₂C₃N₂H₃CH₃⁽¹⁺⁾*Br^(1-)=(CH₃)5C₆CH₂C₃N₂H₃CH₃Br
• Synonyms: (CH₃)5C₆CH₂C₃N₂H₃CH₃⁽¹⁺⁾*Br^(1-)=(CH₃)5C₆CH₂C₃N₂H₃CH₃Br
• CAS NO: 1175017-41-0
• Molecular Weight: 323.276
• Mol File: 1175017-41-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (CH₃)5C₆CH₂C₃N₂H₃CH₃⁽¹⁺⁾*Br^(1-)=(CH₃)5C₆CH₂C₃N₂H₃CH₃Br(CAS DataBase Reference)
• NIST Chemistry Reference: (CH₃)5C₆CH₂C₃N₂H₃CH₃⁽¹⁺⁾*Br^(1-)=(CH₃)5C₆CH₂C₃N₂H₃CH₃Br(1175017-41-0)
• EPA Substance Registry System: (CH₃)5C₆CH₂C₃N₂H₃CH₃⁽¹⁺⁾*Br^(1-)=(CH₃)5C₆CH₂C₃N₂H₃CH₃Br(1175017-41-0)

Safety Data

• Hazardous Substances Data: 1175017-41-0(Hazardous Substances Data)

Upstream product

• 616-47-7 1-methyl-1H-imidazole 
• 53442-65-2 2,3,4,5,6,-pentamethylbenzyl bromide 

Relevant articles and documents

Synthesis, characterization and catalytic activity of N-heterocyclic carbene ligated Schiff base palladacycles

A series of N-heterocyclic carbene (NHC) ligated Schiff base palladacycles were synthesized by the reaction of μ-acetato-bridged Schiff base palladacycles (PdL1-2) with imidazolium salts (a-c). The new NHC ligated palladacycles were fully characterized using 1H NMR, 13C NMR, infrared spectroscopy, MS analysis, and single-crystal X-ray diffraction for one complex (PdL1). Further exploration of the catalytic application of the palladacycles for Suzuki-Miyaura cross-coupling reactions of aryl bromides with phenylboronic acid was carried out. It was determined that the new dimeric imine-palladacycle (PdL2) exhibits the highest catalytic activity among the coupling compounds in this study.