1,1,1-Trifluoro-N-[(11aS)-10,11,12,13-tetrahydro-5-oxido-3,7-bis(2,4,6-trisisopropylphenyl)diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-5-yl]methanesulfonamide
≥98%,≥99% e.e.
- Product Code: 70547
CAS:
1424201-66-0
| Molecular Weight: | 850 g./mol | Molecular Formula: | C₄₈H₅₉F₃NO₅PS |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in advanced organic synthesis, particularly as a specialized ligand or catalyst in asymmetric catalysis. Its unique structure, featuring bulky substituents and a trifluoromethyl group, makes it highly effective in facilitating enantioselective reactions, which are crucial for producing chiral molecules in pharmaceuticals and fine chemicals. The compound's steric and electronic properties enhance selectivity and efficiency in complex transformations, such as carbon-carbon bond formation or hydrogenation processes. Its application is particularly valuable in the development of active pharmaceutical ingredients (APIs) and other high-value compounds requiring precise stereochemical control. Additionally, it may be used in research settings to explore new catalytic mechanisms or optimize reaction conditions for industrial-scale synthesis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿68,000.00 |
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1,1,1-Trifluoro-N-[(11aS)-10,11,12,13-tetrahydro-5-oxido-3,7-bis(2,4,6-trisisopropylphenyl)diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-5-yl]methanesulfonamide
This chemical is primarily utilized in advanced organic synthesis, particularly as a specialized ligand or catalyst in asymmetric catalysis. Its unique structure, featuring bulky substituents and a trifluoromethyl group, makes it highly effective in facilitating enantioselective reactions, which are crucial for producing chiral molecules in pharmaceuticals and fine chemicals. The compound's steric and electronic properties enhance selectivity and efficiency in complex transformations, such as carbon-carbon bond formation or hydrogenation processes. Its application is particularly valuable in the development of active pharmaceutical ingredients (APIs) and other high-value compounds requiring precise stereochemical control. Additionally, it may be used in research settings to explore new catalytic mechanisms or optimize reaction conditions for industrial-scale synthesis.
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