(R)-5-(Chloromethyl)-3-(3-fluoro-4-morpholinophenyl)oxazolidin-2-one
≥95%
- Product Code: 126266
CAS:
496031-57-3
| Molecular Weight: | 314.74 g./mol | Molecular Formula: | C14H16ClFN2O3 |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22683177 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store in inert gas |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of novel antibacterial agents. Its structure is particularly valuable in the development of oxazolidinone-class antibiotics, which are effective against drug-resistant bacterial strains. The presence of the morpholine and fluoro groups enhances its binding affinity to bacterial ribosomes, making it a crucial component in creating drugs targeting Gram-positive pathogens. Additionally, its chiral center allows for the production of enantiomerically pure compounds, which are essential for optimizing drug efficacy and reducing side effects. Research is also ongoing to explore its potential in treating tuberculosis and other complex infections.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white solid |
| Purity (%) | 94.5-100 |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $94.38 |
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| 1.000 | 10-20 days | $279.21 |
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(R)-5-(Chloromethyl)-3-(3-fluoro-4-morpholinophenyl)oxazolidin-2-one
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of novel antibacterial agents. Its structure is particularly valuable in the development of oxazolidinone-class antibiotics, which are effective against drug-resistant bacterial strains. The presence of the morpholine and fluoro groups enhances its binding affinity to bacterial ribosomes, making it a crucial component in creating drugs targeting Gram-positive pathogens. Additionally, its chiral center allows for the production of enantiomerically pure compounds, which are essential for optimizing drug efficacy and reducing side effects. Research is also ongoing to explore its potential in treating tuberculosis and other complex infections.
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