2-[Bis(3,5-di-t-butyl-4-methoxyphenyl)phosphino]benzaldehyde
98%
- Product Code: 68771
CAS:
1202865-21-1
| Molecular Weight: | 574.77 g./mol | Molecular Formula: | C₃₇H₅₁O₃P |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD15143663 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, airtight, dry |
Product Description:
This chemical is primarily used as a ligand in catalytic processes, particularly in transition metal-catalyzed reactions. It is effective in facilitating cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, due to its sterically hindered and electron-rich phosphine structure. The compound enhances the stability and activity of metal catalysts, improving reaction efficiency and selectivity. It is also employed in asymmetric synthesis, where its chiral environment aids in producing enantiomerically pure compounds. Additionally, its application extends to materials science, where it is used in the development of advanced polymers and coordination complexes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,318.00 |
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| 0.250 | 10-20 days | ฿12,672.00 |
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| 1.000 | 10-20 days | ฿42,372.00 |
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2-[Bis(3,5-di-t-butyl-4-methoxyphenyl)phosphino]benzaldehyde
This chemical is primarily used as a ligand in catalytic processes, particularly in transition metal-catalyzed reactions. It is effective in facilitating cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, due to its sterically hindered and electron-rich phosphine structure. The compound enhances the stability and activity of metal catalysts, improving reaction efficiency and selectivity. It is also employed in asymmetric synthesis, where its chiral environment aids in producing enantiomerically pure compounds. Additionally, its application extends to materials science, where it is used in the development of advanced polymers and coordination complexes.
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