Palladium, [1,3-bis[2,6-bis(1-methylethyl)phenyl]-1,3-dihydro-2H-imidazol-2-ylidene]dichloro(1-methyl-1H-imidazole-kN3)-, (SP-4-1)-

97%

  • Product Code: 52749
  CAS:    1314876-23-7
Molecular Weight: 648.02 g./mol Molecular Formula: C₃₁H₄₂Cl₂N₄Pd
EC Number: MDL Number: MFCD28252260
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C, store under inert gas
Product Description: This palladium complex is widely used as a highly efficient catalyst in various organic synthesis reactions, particularly in cross-coupling reactions such as Suzuki-Miyaura, Heck, and Sonogashira couplings. Its robust structure and stability make it suitable for catalyzing the formation of carbon-carbon and carbon-heteroatom bonds, which are essential in the production of pharmaceuticals, agrochemicals, and advanced materials. The complex is also employed in asymmetric synthesis, enabling the creation of chiral molecules with high enantioselectivity, which is crucial in drug development. Additionally, it is utilized in polymer chemistry for the polymerization of olefins and other monomers, contributing to the development of specialized polymers with tailored properties. Its versatility and effectiveness under mild reaction conditions make it a valuable tool in both academic research and industrial applications.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿12,960.00
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0.250 10-20 days ฿25,920.00
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Palladium, [1,3-bis[2,6-bis(1-methylethyl)phenyl]-1,3-dihydro-2H-imidazol-2-ylidene]dichloro(1-methyl-1H-imidazole-kN3)-, (SP-4-1)-
This palladium complex is widely used as a highly efficient catalyst in various organic synthesis reactions, particularly in cross-coupling reactions such as Suzuki-Miyaura, Heck, and Sonogashira couplings. Its robust structure and stability make it suitable for catalyzing the formation of carbon-carbon and carbon-heteroatom bonds, which are essential in the production of pharmaceuticals, agrochemicals, and advanced materials. The complex is also employed in asymmetric synthesis, enabling the creation of chiral molecules with high enantioselectivity, which is crucial in drug development. Additionally, it is utilized in polymer chemistry for the polymerization of olefins and other monomers, contributing to the development of specialized polymers with tailored properties. Its versatility and effectiveness under mild reaction conditions make it a valuable tool in both academic research and industrial applications.
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