1,1'-(2,6-Pyridinediyl)bis(3-methylimidazolium) Dibromide

98%

  • Product Code: 69003
  CAS:    263874-05-1
Molecular Weight: 401.11 g./mol Molecular Formula: C₁₃H₁₅Br₂N₅
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: This chemical is primarily utilized in the field of catalysis, particularly as a precursor for the synthesis of N-heterocyclic carbene (NHC) complexes. These complexes are widely employed in organic synthesis, including cross-coupling reactions, due to their stability and efficiency in facilitating various chemical transformations. Additionally, it finds application in the development of ionic liquids, which are used as solvents or electrolytes in electrochemical devices, such as batteries and fuel cells, owing to their low volatility and high thermal stability. Its structure also makes it a candidate for research in supramolecular chemistry, where it can be used to design and study molecular recognition systems.
Product Specification:
Test Specification
APPEARANCE White to Light yellow to Light orange powder to crystal
PURITY 97.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.050 10-20 days ฿621.00
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-
0.250 10-20 days ฿2,169.00
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-
1.000 10-20 days ฿6,810.00
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1,1'-(2,6-Pyridinediyl)bis(3-methylimidazolium) Dibromide
This chemical is primarily utilized in the field of catalysis, particularly as a precursor for the synthesis of N-heterocyclic carbene (NHC) complexes. These complexes are widely employed in organic synthesis, including cross-coupling reactions, due to their stability and efficiency in facilitating various chemical transformations. Additionally, it finds application in the development of ionic liquids, which are used as solvents or electrolytes in electrochemical devices, such as batteries and fuel cells, owing to their low volatility and high thermal stability. Its structure also makes it a candidate for research in supramolecular chemistry, where it can be used to design and study molecular recognition systems.
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