Di-μ-chlorotetrakis[3,5-difluoro-2-(2-pyridinyl-κN)phenyl-κC

98%

  • Product Code: 94265
  CAS:    562824-27-5
Molecular Weight: 1216.030 g./mol Molecular Formula: C₄₄H₂₄Cl₂F₈Ir₂N₄
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Density: Storage Condition: 2-8°C, inert gas
Product Description: This chemical is primarily utilized in the field of organic synthesis and catalysis, particularly in cross-coupling reactions. It serves as an effective catalyst in the formation of carbon-carbon and carbon-heteroatom bonds, which are essential in the production of pharmaceuticals, agrochemicals, and advanced materials. Its unique structure, featuring a palladium center with bridging chloride ligands and pyridinyl-phenyl groups, enhances its stability and reactivity under various reaction conditions. Additionally, it is employed in the development of luminescent materials and coordination polymers due to its ability to form complex structures with interesting photophysical properties. Its application in asymmetric synthesis also makes it valuable for producing chiral compounds with high enantioselectivity.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿2,457.00
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0.250 10-20 days ฿4,185.00
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1.000 10-20 days ฿12,600.00
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Di-μ-chlorotetrakis[3,5-difluoro-2-(2-pyridinyl-κN)phenyl-κC
This chemical is primarily utilized in the field of organic synthesis and catalysis, particularly in cross-coupling reactions. It serves as an effective catalyst in the formation of carbon-carbon and carbon-heteroatom bonds, which are essential in the production of pharmaceuticals, agrochemicals, and advanced materials. Its unique structure, featuring a palladium center with bridging chloride ligands and pyridinyl-phenyl groups, enhances its stability and reactivity under various reaction conditions. Additionally, it is employed in the development of luminescent materials and coordination polymers due to its ability to form complex structures with interesting photophysical properties. Its application in asymmetric synthesis also makes it valuable for producing chiral compounds with high enantioselectivity.
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