(4S,4'S)-4,4'-Di((S)-sec-butyl)-4,4',5,5'-tetrahydro-2,2'-bioxazole
97%
- Product Code: 69786
CAS:
133463-89-5
| Molecular Weight: | 252.35 g./mol | Molecular Formula: | C₁₄H₂₄N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD33022379 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, stored under inert gas |
Product Description:
Used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It plays a significant role in the formation of chiral centers in organic molecules, aiding in the production of pharmaceuticals and fine chemicals with high enantiomeric purity. Its application extends to hydrogenation and other transition metal-catalyzed processes, enhancing the efficiency and selectivity of these reactions. Additionally, it is employed in the development of advanced materials and agrochemicals, where precise stereochemical control is essential.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,204.00 |
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| 0.250 | 10-20 days | ฿7,074.00 |
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| 1.000 | 10-20 days | ฿22,221.00 |
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(4S,4'S)-4,4'-Di((S)-sec-butyl)-4,4',5,5'-tetrahydro-2,2'-bioxazole
Used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It plays a significant role in the formation of chiral centers in organic molecules, aiding in the production of pharmaceuticals and fine chemicals with high enantiomeric purity. Its application extends to hydrogenation and other transition metal-catalyzed processes, enhancing the efficiency and selectivity of these reactions. Additionally, it is employed in the development of advanced materials and agrochemicals, where precise stereochemical control is essential.
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