1,3-Bis(2,6-dibenzhydryl-4-methylphenyl)-1H-imidazol-3-ium chloride

95%

  • Product Code: 152290
  CAS:    1218778-19-8
Molecular Weight: 949.66 g./mol Molecular Formula: C₆₉H₅₇ClN₂
EC Number: MDL Number: MFCD31580175
Melting Point: Boiling Point:
Density: Storage Condition: Room temperature, avoid light
Product Description: Widely used as a precursor for N-heterocyclic carbene (NHC) ligands in organometallic catalysis. It plays a key role in the development of highly active and selective transition metal catalysts, especially in cross-coupling reactions such as Suzuki-Miyaura and Heck reactions. The bulky dibenzhydryl groups enhance steric protection around the metal center, improving catalyst stability and preventing unwanted side reactions. It is particularly valued in ruthenium- and palladium-based catalytic systems for olefin metathesis and C–C bond formation. Due to its strong electron-donating properties, it helps increase catalytic efficiency under mild conditions, making it useful in pharmaceutical synthesis and fine chemical manufacturing.
Sizes / Availability / Pricing:
Size Availability Price Quantity
0.100 10-20 days $276.39
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0.250 10-20 days $458.53
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1.000 10-20 days $1,478.95
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1,3-Bis(2,6-dibenzhydryl-4-methylphenyl)-1H-imidazol-3-ium chloride
Widely used as a precursor for N-heterocyclic carbene (NHC) ligands in organometallic catalysis. It plays a key role in the development of highly active and selective transition metal catalysts, especially in cross-coupling reactions such as Suzuki-Miyaura and Heck reactions. The bulky dibenzhydryl groups enhance steric protection around the metal center, improving catalyst stability and preventing unwanted side reactions. It is particularly valued in ruthenium- and palladium-based catalytic systems for olefin metathesis and C–C bond formation. Due to its strong electron-donating properties, it helps increase catalytic efficiency under mild conditions, making it useful in pharmaceutical synthesis and fine chemical manufacturing.
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