(S)-N-[3-(3-FLUORO-4-IODO-PHENYL)-2-OXO-OXAZOLIDIN-5-YLMETHYL]-ACETAMIDE
98%
- Product Code: 38626
CAS:
149524-45-8
| Molecular Weight: | 378.14 g./mol | Molecular Formula: | C₁₂H₁₂FIN₂O₃ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 520.6±40.0℃(Predicted) | |
| Density: | 1.736±0.06 g/cm3(Predicted) | Storage Condition: | 2-8℃, dry |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of biologically active molecules. Its structure, featuring a fluorinated and iodinated phenyl ring along with an oxazolidinone core, makes it valuable for developing novel pharmaceuticals, particularly antibiotics. The oxazolidinone moiety is known for its role in inhibiting bacterial protein synthesis, making it a key component in the design of drugs targeting resistant bacterial strains. Additionally, the presence of fluorine and iodine atoms enhances the compound's ability to interact with biological targets, improving binding affinity and pharmacokinetic properties. It is often employed in research to explore new treatments for infections caused by Gram-positive bacteria, including MRSA and other multidrug-resistant pathogens.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,297.00 |
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| 0.250 | 10-20 days | ฿10,656.00 |
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| 1.000 | 10-20 days | ฿21,312.00 |
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(S)-N-[3-(3-FLUORO-4-IODO-PHENYL)-2-OXO-OXAZOLIDIN-5-YLMETHYL]-ACETAMIDE
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of biologically active molecules. Its structure, featuring a fluorinated and iodinated phenyl ring along with an oxazolidinone core, makes it valuable for developing novel pharmaceuticals, particularly antibiotics. The oxazolidinone moiety is known for its role in inhibiting bacterial protein synthesis, making it a key component in the design of drugs targeting resistant bacterial strains. Additionally, the presence of fluorine and iodine atoms enhances the compound's ability to interact with biological targets, improving binding affinity and pharmacokinetic properties. It is often employed in research to explore new treatments for infections caused by Gram-positive bacteria, including MRSA and other multidrug-resistant pathogens.
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