5-(3-Bromophenyl)oxazolidin-2-one
≥95%
- Product Code: 82587
CAS:
943910-36-9
| Molecular Weight: | 242.07 g./mol | Molecular Formula: | C₉H₈BrNO₂ |
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| EC Number: | MDL Number: | MFCD16321849 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure, featuring a bromophenyl group attached to an oxazolidinone ring, makes it valuable for constructing more complex molecules, particularly those with potential biological activity. It is often employed in the development of antibacterial agents, as the oxazolidinone core is known for its efficacy in inhibiting bacterial protein synthesis. Additionally, the bromine atom provides a reactive site for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery. Its role in medicinal chemistry is significant, particularly in the design of new therapeutic compounds targeting resistant bacterial strains.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft101,815.32 |
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| 0.250 | 10-20 days | Ft169,013.43 |
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5-(3-Bromophenyl)oxazolidin-2-one
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure, featuring a bromophenyl group attached to an oxazolidinone ring, makes it valuable for constructing more complex molecules, particularly those with potential biological activity. It is often employed in the development of antibacterial agents, as the oxazolidinone core is known for its efficacy in inhibiting bacterial protein synthesis. Additionally, the bromine atom provides a reactive site for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery. Its role in medicinal chemistry is significant, particularly in the design of new therapeutic compounds targeting resistant bacterial strains.
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