1-[(4S)-4-(phenylMethyl)-2-thioxo-3-oxazolidinyl]-Ethanone
98%
- Product Code: 70577
CAS:
694520-56-4
| Molecular Weight: | 235.30212 g./mol | Molecular Formula: | C₁₂H₁₃NO₂S |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmacologically active compounds. Its structure, featuring a thioxo-oxazolidinyl group, makes it particularly valuable in the development of new drugs, especially those targeting bacterial infections. Researchers often employ it in the synthesis of oxazolidinone derivatives, which are known for their potent antibacterial properties. Additionally, its phenylmethyl group enhances its reactivity, allowing for further functionalization to create more complex molecules. This compound is also explored in the study of enzyme inhibition, where it can act as a scaffold for designing inhibitors that target specific enzymes involved in disease pathways. Its versatility in chemical reactions makes it a valuable tool in medicinal chemistry and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿14,760.00 |
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| 0.250 | 10-20 days | ฿22,185.00 |
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1-[(4S)-4-(phenylMethyl)-2-thioxo-3-oxazolidinyl]-Ethanone
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmacologically active compounds. Its structure, featuring a thioxo-oxazolidinyl group, makes it particularly valuable in the development of new drugs, especially those targeting bacterial infections. Researchers often employ it in the synthesis of oxazolidinone derivatives, which are known for their potent antibacterial properties. Additionally, its phenylmethyl group enhances its reactivity, allowing for further functionalization to create more complex molecules. This compound is also explored in the study of enzyme inhibition, where it can act as a scaffold for designing inhibitors that target specific enzymes involved in disease pathways. Its versatility in chemical reactions makes it a valuable tool in medicinal chemistry and drug discovery.
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