1,3-Bis(2,6-di-i-propylphenyl)imidazol-2-ylidene(1,4-naphthoquinone)palladium (0) dimer

96%

  • Product Code: 126325
  CAS:    649736-75-4
Molecular Weight: 1306.3199 g./mol Molecular Formula: C74H84N4O4Pd2
EC Number: MDL Number: MFCD09752621
Melting Point: Boiling Point:
Density: Storage Condition: Room temperature, sealed, dry
Product Description: This chemical is primarily utilized as a highly efficient catalyst in various organic synthesis reactions, particularly in cross-coupling processes. Its application is prominent in the formation of carbon-carbon and carbon-heteroatom bonds, which are fundamental in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound's stability and reactivity make it suitable for use in challenging reactions, including those requiring mild conditions or involving sensitive substrates. Additionally, it is employed in the synthesis of complex organic molecules, where its ability to facilitate selective transformations is highly valued. Its use in industrial and academic research underscores its importance in advancing synthetic methodologies.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days $126.61
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0.250 10-20 days $232.82
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1,3-Bis(2,6-di-i-propylphenyl)imidazol-2-ylidene(1,4-naphthoquinone)palladium (0) dimer
This chemical is primarily utilized as a highly efficient catalyst in various organic synthesis reactions, particularly in cross-coupling processes. Its application is prominent in the formation of carbon-carbon and carbon-heteroatom bonds, which are fundamental in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound's stability and reactivity make it suitable for use in challenging reactions, including those requiring mild conditions or involving sensitive substrates. Additionally, it is employed in the synthesis of complex organic molecules, where its ability to facilitate selective transformations is highly valued. Its use in industrial and academic research underscores its importance in advancing synthetic methodologies.
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