1,4-Bis(diphenylphosphino)butane
98%
- Product Code: 68732
Alias:
1,4-bis(diphenylphosphino)butane
CAS:
7688-25-7
| Molecular Weight: | 426.47 g./mol | Molecular Formula: | C₂₈H₂₈P₂ |
|---|---|---|---|
| EC Number: | 231-698-7 | MDL Number: | MFCD00003051 |
| Melting Point: | 132-136 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
1,4-Bis(diphenylphosphino)butane is widely used as a ligand in coordination chemistry and catalysis. It plays a significant role in the formation of transition metal complexes, particularly in palladium-catalyzed cross-coupling reactions, such as Suzuki and Heck reactions, which are essential in organic synthesis for creating carbon-carbon bonds. Its bidentate structure allows it to stabilize metal centers effectively, enhancing catalytic activity and selectivity. Additionally, it is employed in the synthesis of organometallic compounds and in asymmetric hydrogenation processes, contributing to the production of chiral molecules in pharmaceuticals and fine chemicals. Its versatility and stability make it a valuable tool in both academic research and industrial applications.
Product Specification:
| Test | Specification |
|---|---|
| PURITY HPLC | 98-100 |
| MELTING POINT | 132-136 |
| APPEARANCE COLOR | White |
| APPEARANCE FORM | Powder or Crystalline Powder |
| INFRARED SPECTRUM | Conforms to Structure |
| SOLUBILITY TURBIDITY | Clear to Very Slightly Hazy 2.5% in Chloroform |
| SOLUBILITY COLOR | COLORLESS TO VERY FAINT YELLOW |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿420.00 |
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| 25.000 | 10-20 days | ฿980.00 |
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| 100.000 | 10-20 days | ฿2,970.00 |
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| 500.000 | 10-20 days | ฿12,820.00 |
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1,4-Bis(diphenylphosphino)butane
1,4-Bis(diphenylphosphino)butane is widely used as a ligand in coordination chemistry and catalysis. It plays a significant role in the formation of transition metal complexes, particularly in palladium-catalyzed cross-coupling reactions, such as Suzuki and Heck reactions, which are essential in organic synthesis for creating carbon-carbon bonds. Its bidentate structure allows it to stabilize metal centers effectively, enhancing catalytic activity and selectivity. Additionally, it is employed in the synthesis of organometallic compounds and in asymmetric hydrogenation processes, contributing to the production of chiral molecules in pharmaceuticals and fine chemicals. Its versatility and stability make it a valuable tool in both academic research and industrial applications.
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