(R)-3-(4-Bromo-3-fluorophenyl)-5-(hydroxymethyl)oxazolidin-2-one
98%
- Product Code: 37078
CAS:
444335-16-4
| Molecular Weight: | 290.09 g./mol | Molecular Formula: | C₁₀H₉BrFNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08166353 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of biologically active molecules. It plays a significant role in the development of antimicrobial agents, particularly in the creation of oxazolidinone-based antibiotics. These antibiotics are effective against Gram-positive bacteria, including drug-resistant strains like MRSA (Methicillin-Resistant Staphylococcus aureus). Additionally, the compound’s structural features, such as the bromo and fluoro substituents, contribute to its potential use in designing targeted therapies for various bacterial infections. Its hydroxymethyl group also allows for further chemical modifications, making it a versatile building block in medicinal chemistry for optimizing drug efficacy and pharmacokinetic properties.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to light yellow Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿950.00 |
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| 5.000 | 10-20 days | ฿3,420.00 |
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(R)-3-(4-Bromo-3-fluorophenyl)-5-(hydroxymethyl)oxazolidin-2-one
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of biologically active molecules. It plays a significant role in the development of antimicrobial agents, particularly in the creation of oxazolidinone-based antibiotics. These antibiotics are effective against Gram-positive bacteria, including drug-resistant strains like MRSA (Methicillin-Resistant Staphylococcus aureus). Additionally, the compound’s structural features, such as the bromo and fluoro substituents, contribute to its potential use in designing targeted therapies for various bacterial infections. Its hydroxymethyl group also allows for further chemical modifications, making it a versatile building block in medicinal chemistry for optimizing drug efficacy and pharmacokinetic properties.
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