(S)-2,2'-Bis[bis(4-methoxy-3,5-dimethylphenyl)phosphino]-4,4',6,6'-tetramethoxy)-1,1'-biphenyl
98%,99%ee
- Product Code: 37998
CAS:
1365531-94-7
| Molecular Weight: | 874.9800 g./mol | Molecular Formula: | C₅₂H₆₀O₈P₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD19443626 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its structure, featuring electron-rich phosphine groups and methoxy substituents, makes it highly effective in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. It is often employed in the synthesis of pharmaceuticals and fine chemicals, where high enantiomeric purity is critical. The ligand’s steric and electronic properties enhance the selectivity and efficiency of the catalytic process, making it a valuable tool in organic synthesis and industrial applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,752.00 |
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(S)-2,2'-Bis[bis(4-methoxy-3,5-dimethylphenyl)phosphino]-4,4',6,6'-tetramethoxy)-1,1'-biphenyl
This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its structure, featuring electron-rich phosphine groups and methoxy substituents, makes it highly effective in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. It is often employed in the synthesis of pharmaceuticals and fine chemicals, where high enantiomeric purity is critical. The ligand’s steric and electronic properties enhance the selectivity and efficiency of the catalytic process, making it a valuable tool in organic synthesis and industrial applications.
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