1,1'-[(5aR,8aR,14aR)-5a,6,7,8,8a,9-hexahydro-5H-[1]benzopyrano[3,2-d]xanthene-1,13-diyl]bis[1,1-di(4-methylphenyl)phosphine]
≥95%,≥99%e.e.
- Product Code: 70535
CAS:
1429939-32-1
| Molecular Weight: | 716.8 g./mol | Molecular Formula: | C₄₈H₄₆O₂P₂ |
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| EC Number: | MDL Number: | ||
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly as a ligand in catalytic processes. Its unique structure, featuring phosphine groups, makes it highly effective in facilitating various transition metal-catalyzed reactions, such as cross-coupling reactions, which are essential in the production of pharmaceuticals, agrochemicals, and advanced materials. The steric and electronic properties of the ligand enhance the stability and activity of the metal catalysts, leading to improved reaction efficiency and selectivity. Additionally, its application extends to asymmetric synthesis, where it aids in the creation of chiral compounds with high enantiomeric purity, crucial for the development of active pharmaceutical ingredients (APIs).
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿8,220.00 |
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| 0.100 | 10-20 days | ฿12,320.00 |
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1,1'-[(5aR,8aR,14aR)-5a,6,7,8,8a,9-hexahydro-5H-[1]benzopyrano[3,2-d]xanthene-1,13-diyl]bis[1,1-di(4-methylphenyl)phosphine]
This chemical is primarily utilized in the field of organic synthesis, particularly as a ligand in catalytic processes. Its unique structure, featuring phosphine groups, makes it highly effective in facilitating various transition metal-catalyzed reactions, such as cross-coupling reactions, which are essential in the production of pharmaceuticals, agrochemicals, and advanced materials. The steric and electronic properties of the ligand enhance the stability and activity of the metal catalysts, leading to improved reaction efficiency and selectivity. Additionally, its application extends to asymmetric synthesis, where it aids in the creation of chiral compounds with high enantiomeric purity, crucial for the development of active pharmaceutical ingredients (APIs).
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