Tris(dibenzylideneacetone)dipalladium(0)-chloroform adduct
98%
- Product Code: 68367
Alias:
Tris(dibenzylideneacetone)dipalladium, chloroform adduct; Tris(dibenzylideneacetone)dipalladium chloroform complex
CAS:
52522-40-4
| Molecular Weight: | 1035.1 g./mol | Molecular Formula: | C₅₂H₄₃Cl₃O₃Pd₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00075479 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2~8°C |
Product Description:
Widely used in organic synthesis as a catalyst, particularly in cross-coupling reactions like Suzuki, Heck, and Sonogashira reactions. It facilitates the formation of carbon-carbon bonds, making it essential in the production of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity in chloroform make it a preferred choice for homogeneous catalysis. Additionally, it is employed in the synthesis of complex organic molecules and polymers, contributing to advancements in material science and drug development.
Product Specification:
| Test | Specification |
|---|---|
| Pd | 20.1-20.9 |
| PURITYEX Pd | 98-100 |
| APPEARANCE | PURPLE TO BLACK POWDER,CRYSTALS,FLAKES OR CHIPS |
| INFRARED SPECTROMETRY | Conforms to Structure |
| TOTAL METALLIC IMPURITIES | 1600ppm |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,820.00 |
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| 1.000 | 10-20 days | ฿4,650.00 |
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| 5.000 | 10-20 days | ฿18,690.00 |
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Tris(dibenzylideneacetone)dipalladium(0)-chloroform adduct
Widely used in organic synthesis as a catalyst, particularly in cross-coupling reactions like Suzuki, Heck, and Sonogashira reactions. It facilitates the formation of carbon-carbon bonds, making it essential in the production of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity in chloroform make it a preferred choice for homogeneous catalysis. Additionally, it is employed in the synthesis of complex organic molecules and polymers, contributing to advancements in material science and drug development.
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