Tris(dibenzylideneacetone)dipalladium(0)
97%
- Product Code: 68363
Alias:
Double [three (dibenzylideneacetone) palladium (0)] 2 palladium (DBA)
CAS:
51364-51-3
Molecular Weight: | 915.72 g./mol | Molecular Formula: | C₅₁H₄₂O₃Pd₂ |
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EC Number: | MDL Number: | MFCD00013310 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2~8°C, sealed, protected from light |
Product Description:
Tris(dibibenzylideneacetone)dipalladium(0) is widely used as a catalyst in various organic synthesis reactions, particularly in cross-coupling reactions such as Suzuki-Miyaura, Heck, and Sonogashira couplings. Its effectiveness in facilitating the formation of carbon-carbon bonds makes it a valuable tool in the synthesis of pharmaceuticals, agrochemicals, and complex organic molecules. Additionally, it is employed in the preparation of fine chemicals and materials science, where precise control over molecular structures is required. The compound's stability and reactivity under mild conditions further enhance its utility in both academic research and industrial applications.
Product Specification:
Test | Specification |
---|---|
Purity | 97 100% |
Pd | 21.5 |
TOTAL METALLIC IMPURITIESPPM | 1600 |
A single impurity contentppm | 100 |
APPEARANCE | RED TO BLACK POWDERAND/OR CRYSTALS |
INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿4,980.00 |
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5.000 | 10-20 days | ฿16,980.00 |
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25.000 | 10-20 days | ฿69,980.00 |
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Tris(dibenzylideneacetone)dipalladium(0)
Tris(dibibenzylideneacetone)dipalladium(0) is widely used as a catalyst in various organic synthesis reactions, particularly in cross-coupling reactions such as Suzuki-Miyaura, Heck, and Sonogashira couplings. Its effectiveness in facilitating the formation of carbon-carbon bonds makes it a valuable tool in the synthesis of pharmaceuticals, agrochemicals, and complex organic molecules. Additionally, it is employed in the preparation of fine chemicals and materials science, where precise control over molecular structures is required. The compound's stability and reactivity under mild conditions further enhance its utility in both academic research and industrial applications.
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