[S(R)]-N-[(S)-(3,5-Di-tert-butyl-4-methoxyphenyl)[2-(di-tert-butylphosphino)phenyl]methyl]-2-methyl-2-propanesulfinamide
≥95%
- Product Code: 68851
CAS:
2565792-54-1
| Molecular Weight: | 573.85 g./mol | Molecular Formula: | C₃₄H₅₆NO₂PS |
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| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in asymmetric synthesis, particularly as a chiral ligand in transition metal-catalyzed reactions. Its unique structure, featuring tert-butyl groups and a sulfinamide moiety, makes it highly effective in inducing enantioselectivity in various organic transformations. It is commonly employed in the synthesis of complex molecules, including pharmaceuticals and fine chemicals, where precise control over stereochemistry is crucial. The compound’s sterically demanding and electron-rich environment enhances its ability to stabilize metal complexes, improving catalytic efficiency and selectivity. Additionally, it is used in the development of novel catalytic systems for C-C and C-X bond-forming reactions, contributing to advancements in synthetic organic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿13,797.00 |
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[S(R)]-N-[(S)-(3,5-Di-tert-butyl-4-methoxyphenyl)[2-(di-tert-butylphosphino)phenyl]methyl]-2-methyl-2-propanesulfinamide
This compound is primarily utilized in asymmetric synthesis, particularly as a chiral ligand in transition metal-catalyzed reactions. Its unique structure, featuring tert-butyl groups and a sulfinamide moiety, makes it highly effective in inducing enantioselectivity in various organic transformations. It is commonly employed in the synthesis of complex molecules, including pharmaceuticals and fine chemicals, where precise control over stereochemistry is crucial. The compound’s sterically demanding and electron-rich environment enhances its ability to stabilize metal complexes, improving catalytic efficiency and selectivity. Additionally, it is used in the development of novel catalytic systems for C-C and C-X bond-forming reactions, contributing to advancements in synthetic organic chemistry.
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