(S)-4-Benzyl-3-(7-bromoheptanoyl)oxazolidin-2-one
95%
- Product Code: 82111
CAS:
203739-35-9
| Molecular Weight: | 368.27 g./mol | Molecular Formula: | C₁₇H₂₂BrNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30471813 | |
| Melting Point: | Boiling Point: | 498.1±28.0 °C(Predicted) | |
| Density: | 1.351±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, inert atmosphere |
Product Description:
This compound is primarily utilized in organic synthesis as a chiral auxiliary. It helps in the stereoselective formation of carbon-carbon bonds, particularly in asymmetric aldol reactions. The (S)-configuration of the oxazolidinone ring ensures high enantioselectivity, making it valuable for producing optically active intermediates in pharmaceuticals. Its application is also seen in the synthesis of complex natural products and bioactive molecules, where precise control over stereochemistry is crucial. The bromoheptanoyl moiety provides a reactive site for further functionalization, enabling the construction of diverse molecular architectures.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿20,250.00 |
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| 0.250 | 10-20 days | ฿37,800.00 |
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(S)-4-Benzyl-3-(7-bromoheptanoyl)oxazolidin-2-one
This compound is primarily utilized in organic synthesis as a chiral auxiliary. It helps in the stereoselective formation of carbon-carbon bonds, particularly in asymmetric aldol reactions. The (S)-configuration of the oxazolidinone ring ensures high enantioselectivity, making it valuable for producing optically active intermediates in pharmaceuticals. Its application is also seen in the synthesis of complex natural products and bioactive molecules, where precise control over stereochemistry is crucial. The bromoheptanoyl moiety provides a reactive site for further functionalization, enabling the construction of diverse molecular architectures.
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