(4S,4'S)-2,2'-(Pentane-3,3'-diyl)bis(4-benzyl-4,5-dihydrooxazole)
98.0%
- Product Code: 69728
CAS:
160191-64-0
| Molecular Weight: | 390.53 g./mol | Molecular Formula: | C₂₅H₃₀N₂O₂ |
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| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, where it helps in the formation of chiral centers with high enantiomeric excess. Its structure, featuring a bis(oxazoline) framework, makes it effective in coordinating with metals like copper, palladium, and rhodium, enhancing the efficiency and selectivity of the catalytic system. Additionally, it finds application in the synthesis of pharmaceuticals and fine chemicals, where precise control over stereochemistry is essential. Its robust and tunable nature allows for its use in a variety of complex organic transformations.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Pale yellow - Deep yellow Liquid |
| PURITY | 98-100 |
| SPECIFIC ROTATION A20DC2.5 CHCL3 | -23--20 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿5,580.00 |
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| 1.000 | 10-20 days | ฿22,005.00 |
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(4S,4'S)-2,2'-(Pentane-3,3'-diyl)bis(4-benzyl-4,5-dihydrooxazole)
This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, where it helps in the formation of chiral centers with high enantiomeric excess. Its structure, featuring a bis(oxazoline) framework, makes it effective in coordinating with metals like copper, palladium, and rhodium, enhancing the efficiency and selectivity of the catalytic system. Additionally, it finds application in the synthesis of pharmaceuticals and fine chemicals, where precise control over stereochemistry is essential. Its robust and tunable nature allows for its use in a variety of complex organic transformations.
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