[1,1'-Bis(diphenylphosphino)ferrocene]dichloropalladium(II)
Pd 14.5%
- Product Code: 126706
Alias:
[1,1'-Bis(diphenylphosphino)ferrocene]palladium dichloride
CAS:
72287-26-4
Molecular Weight: | 731.7 g./mol | Molecular Formula: | C₃₄H₂₈Cl₂FeP₂Pd |
---|---|---|---|
EC Number: | MDL Number: | MFCD00015757 | |
Melting Point: | 275-280 °C(lit.) | Boiling Point: | |
Density: | Storage Condition: | room temperature |
Product Description:
This chemical is widely used as a catalyst in various organic synthesis reactions, particularly in cross-coupling reactions such as Suzuki-Miyaura and Heck reactions. Its effectiveness stems from the stability and versatility provided by the ferrocene backbone and the diphenylphosphine ligands, which enhance the catalytic activity of palladium. It is especially valuable in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The compound’s ability to facilitate the formation of carbon-carbon and carbon-heteroatom bonds makes it a key tool in modern synthetic chemistry. Additionally, its use in asymmetric catalysis enables the production of enantiomerically pure compounds, which are crucial in drug development and fine chemical manufacturing.
Product Specification:
Test | Specification |
---|---|
Assay (Pd%) | 13-15 |
Appearance | Red To Dark Brown Powder |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
---|---|---|---|
1.000 | 10-20 days | ฿4,530.00 |
+
-
|
5.000 | 10-20 days | ฿16,910.00 |
+
-
|
25.000 | 10-20 days | ฿65,370.00 |
+
-
|
[1,1'-Bis(diphenylphosphino)ferrocene]dichloropalladium(II)
This chemical is widely used as a catalyst in various organic synthesis reactions, particularly in cross-coupling reactions such as Suzuki-Miyaura and Heck reactions. Its effectiveness stems from the stability and versatility provided by the ferrocene backbone and the diphenylphosphine ligands, which enhance the catalytic activity of palladium. It is especially valuable in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The compound’s ability to facilitate the formation of carbon-carbon and carbon-heteroatom bonds makes it a key tool in modern synthetic chemistry. Additionally, its use in asymmetric catalysis enables the production of enantiomerically pure compounds, which are crucial in drug development and fine chemical manufacturing.
Mechanism | - |
Appearance | - |
Longevity | - |
Strength | - |
Storage | - |
Shelf Life | - |
Allergen(s) | - |
Dosage (Range) | - |
Recommended Dosage | - |
Dosage (Per Day) | - |
Recommended Dosage (Per Day) | - |
Mix Method | - |
Heat Resistance | - |
Stable in pH range | - |
Solubility | - |
Product Types | - |
INCI | - |
Cart
No products
Subtotal:
฿0.00
฿0.00
Total :