(R)-4-Benzyl-3-(3-methylbutanoyl)oxazolidin-2-one
97%
- Product Code: 117648
CAS:
145589-03-3
| Molecular Weight: | 261.32 g./mol | Molecular Formula: | C₁₅H₁₉NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD10566718 | |
| Melting Point: | Boiling Point: | 412.9°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized as a chiral auxiliary in asymmetric synthesis, enabling the production of enantiomerically pure substances. It is particularly effective in controlling stereochemistry during the formation of carbon-carbon bonds, such as in aldol reactions, alkylations, and Diels-Alder reactions. Its rigid structure and ability to induce high enantioselectivity make it a valuable tool in the synthesis of complex molecules, including pharmaceuticals and natural products. Additionally, it is employed in the preparation of intermediates for drug development, where precise stereochemical control is critical for biological activity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | Ft2,909.01 |
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| 1.000 | 10-20 days | Ft7,757.36 |
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| 5.000 | 10-20 days | Ft21,623.63 |
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(R)-4-Benzyl-3-(3-methylbutanoyl)oxazolidin-2-one
This compound is primarily utilized as a chiral auxiliary in asymmetric synthesis, enabling the production of enantiomerically pure substances. It is particularly effective in controlling stereochemistry during the formation of carbon-carbon bonds, such as in aldol reactions, alkylations, and Diels-Alder reactions. Its rigid structure and ability to induce high enantioselectivity make it a valuable tool in the synthesis of complex molecules, including pharmaceuticals and natural products. Additionally, it is employed in the preparation of intermediates for drug development, where precise stereochemical control is critical for biological activity.
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