(R)-()-4-benzyl-5,5-dimethyl-2-oxazol-idinone
98%
- Product Code: 70252
CAS:
204851-73-0
| Molecular Weight: | 205.253 g./mol | Molecular Formula: | C₁₂H₁₅NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 60-62 °C(lit.) | Boiling Point: | 385 °C at 760 mmHg |
| Density: | 1.085±0.06 g/cm3 | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in organic synthesis as a chiral auxiliary. It is employed to induce stereoselectivity in various reactions, particularly in the formation of asymmetric carbon-carbon bonds. Its rigid structure and ability to coordinate with metal catalysts make it valuable in enantioselective transformations. Additionally, it is used in the synthesis of complex molecules, including pharmaceuticals, where controlling the stereochemistry is crucial for biological activity. Its application extends to the preparation of intermediates for natural products and fine chemicals, enhancing the efficiency and selectivity of synthetic routes.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to yellow powder or crystals |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,430.00 |
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| 0.500 | 10-20 days | ฿8,540.00 |
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(R)-()-4-benzyl-5,5-dimethyl-2-oxazol-idinone
This chemical is primarily utilized in organic synthesis as a chiral auxiliary. It is employed to induce stereoselectivity in various reactions, particularly in the formation of asymmetric carbon-carbon bonds. Its rigid structure and ability to coordinate with metal catalysts make it valuable in enantioselective transformations. Additionally, it is used in the synthesis of complex molecules, including pharmaceuticals, where controlling the stereochemistry is crucial for biological activity. Its application extends to the preparation of intermediates for natural products and fine chemicals, enhancing the efficiency and selectivity of synthetic routes.
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