(R)-4-benzyl-3-(2-bromoacetyl)oxazolidin-2-one
95%
- Product Code: 82099
CAS:
110905-24-3
| Molecular Weight: | 298.13 g./mol | Molecular Formula: | C₁₂H₁₂BrNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD29085062 | |
| Melting Point: | 41-42 °C | Boiling Point: | 427.7±28.0 °C(Predicted) |
| Density: | 1.568±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a chiral auxiliary and building block for the preparation of enantiomerically pure compounds. It is often employed in asymmetric synthesis to induce stereoselectivity in reactions, particularly in the formation of carbon-carbon or carbon-heteroatom bonds. The oxazolidinone moiety acts as a directing group, enabling precise control over the stereochemistry of the final product. Its application is common in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where the introduction of chiral centers is critical for biological activity. The bromoacetyl group further enhances its reactivity, allowing for versatile functionalization in multi-step synthetic routes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft119,754.21 |
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| 0.250 | 10-20 days | Ft220,599.86 |
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| 1.000 | 10-20 days | Ft441,199.72 |
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(R)-4-benzyl-3-(2-bromoacetyl)oxazolidin-2-one
This compound is primarily utilized in organic synthesis as a chiral auxiliary and building block for the preparation of enantiomerically pure compounds. It is often employed in asymmetric synthesis to induce stereoselectivity in reactions, particularly in the formation of carbon-carbon or carbon-heteroatom bonds. The oxazolidinone moiety acts as a directing group, enabling precise control over the stereochemistry of the final product. Its application is common in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where the introduction of chiral centers is critical for biological activity. The bromoacetyl group further enhances its reactivity, allowing for versatile functionalization in multi-step synthetic routes.
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