1,2-Bis(bis(3,5-bis(trifluoromethyl)phenyl)phosphanyl)ethane
97%
- Product Code: 38849
CAS:
199342-62-6
| Molecular Weight: | 942.4001 g./mol | Molecular Formula: | C₃₄H₁₆F₂₄P₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01630832 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized as a ligand in catalytic processes, particularly in transition metal catalysis. It is highly effective in facilitating cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, due to its strong electron-withdrawing properties and steric bulk. The trifluoromethyl groups enhance the ligand's stability and reactivity, making it suitable for use in challenging synthetic transformations. Additionally, it is employed in asymmetric catalysis, where it helps achieve high enantioselectivity in the production of chiral compounds. Its robust structure also makes it valuable in industrial applications, including the synthesis of pharmaceuticals, agrochemicals, and advanced materials.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | €68.38 |
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1,2-Bis(bis(3,5-bis(trifluoromethyl)phenyl)phosphanyl)ethane
This chemical is primarily utilized as a ligand in catalytic processes, particularly in transition metal catalysis. It is highly effective in facilitating cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, due to its strong electron-withdrawing properties and steric bulk. The trifluoromethyl groups enhance the ligand's stability and reactivity, making it suitable for use in challenging synthetic transformations. Additionally, it is employed in asymmetric catalysis, where it helps achieve high enantioselectivity in the production of chiral compounds. Its robust structure also makes it valuable in industrial applications, including the synthesis of pharmaceuticals, agrochemicals, and advanced materials.
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