[Di-tert-butyl(chloro)phosphine]palladium(II) Dichloride Dimer

98%,Pd>29.0%

  • Product Code: 68354
  CAS:    386706-33-8
Molecular Weight: 715.95 g./mol Molecular Formula: C₁₆H₃₆Cl₆P₂Pd₂
EC Number: MDL Number: MFCD05664440
Melting Point: 222°C(分解) Boiling Point:
Density: Storage Condition: room temperature, dry
Product Description: This chemical is widely used as a catalyst in various cross-coupling reactions, particularly in organic synthesis. It plays a crucial role in facilitating the formation of carbon-carbon and carbon-heteroatom bonds, making it essential in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its effectiveness in Suzuki-Miyaura, Heck, and Sonogashira reactions is highly valued due to its stability and efficiency under mild conditions. Additionally, it is employed in the synthesis of complex organic molecules, including natural products and polymers, due to its ability to enhance reaction selectivity and yield. Its application in industrial and academic research continues to drive advancements in synthetic chemistry.
Product Specification:
Test Specification
APPEARANCE Light yellow to Amber to Dark green powder to crystal
PURITY 97.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.025 10-20 days ฿3,990.00
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-
0.100 10-20 days ฿9,880.00
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-
0.500 10-20 days ฿29,960.00
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-
[Di-tert-butyl(chloro)phosphine]palladium(II) Dichloride Dimer
This chemical is widely used as a catalyst in various cross-coupling reactions, particularly in organic synthesis. It plays a crucial role in facilitating the formation of carbon-carbon and carbon-heteroatom bonds, making it essential in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its effectiveness in Suzuki-Miyaura, Heck, and Sonogashira reactions is highly valued due to its stability and efficiency under mild conditions. Additionally, it is employed in the synthesis of complex organic molecules, including natural products and polymers, due to its ability to enhance reaction selectivity and yield. Its application in industrial and academic research continues to drive advancements in synthetic chemistry.
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