Bis(ethylenediamine)palladium(II) Dichloride
98%
- Product Code: 68447
CAS:
16483-18-4
Molecular Weight: | 297.52 g./mol | Molecular Formula: | C₄H₁₆Cl₂N₄Pd |
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EC Number: | MDL Number: | MFCD03844778 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature, dry |
Product Description:
Bis(ethylenediamine)palladium(II) Dichloride is widely used as a catalyst in various organic synthesis reactions, particularly in cross-coupling reactions like the Suzuki and Heck reactions, which are essential for forming carbon-carbon bonds in pharmaceuticals and fine chemicals. It is also employed in the preparation of palladium nanoparticles, which have applications in catalysis, electronics, and sensors. Additionally, this compound is utilized in the development of palladium-based materials for hydrogen storage and fuel cell technologies, owing to its ability to interact with hydrogen molecules. Its role in asymmetric synthesis further highlights its importance in producing chiral compounds for drug development and agrochemicals.
Product Specification:
Test | Specification |
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APPEARANCE | Pale yellow - Yellow green Crystal - Powder Solid |
PURITY | 98 100% |
PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.200 | 10-20 days | ฿6,600.00 |
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Bis(ethylenediamine)palladium(II) Dichloride
Bis(ethylenediamine)palladium(II) Dichloride is widely used as a catalyst in various organic synthesis reactions, particularly in cross-coupling reactions like the Suzuki and Heck reactions, which are essential for forming carbon-carbon bonds in pharmaceuticals and fine chemicals. It is also employed in the preparation of palladium nanoparticles, which have applications in catalysis, electronics, and sensors. Additionally, this compound is utilized in the development of palladium-based materials for hydrogen storage and fuel cell technologies, owing to its ability to interact with hydrogen molecules. Its role in asymmetric synthesis further highlights its importance in producing chiral compounds for drug development and agrochemicals.
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