Methyl 3-(5-(2-fluorophenyl)-1,2,4-oxadiazol-3-yl)benzoate
97%
- Product Code: 117468
CAS:
775304-60-4
| Molecular Weight: | 298.27 g./mol | Molecular Formula: | C₁₆H₁₁FN₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09971792 | |
| Melting Point: | Boiling Point: | 457.2±55.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel bioactive molecules. Its structure, featuring a fluorophenyl group and an oxadiazole ring, makes it a valuable intermediate for designing potential drugs targeting neurological disorders and inflammation. Researchers explore its use in creating compounds with enhanced binding affinity to specific receptors or enzymes, which could lead to the development of new therapeutic agents. Additionally, it serves as a key building block in medicinal chemistry for optimizing drug candidates with improved efficacy and reduced side effects. Its application extends to the study of structure-activity relationships (SAR) to better understand how chemical modifications influence biological activity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿630.00 |
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| 0.250 | 10-20 days | ฿1,080.00 |
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| 1.000 | 10-20 days | ฿2,682.00 |
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Methyl 3-(5-(2-fluorophenyl)-1,2,4-oxadiazol-3-yl)benzoate
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel bioactive molecules. Its structure, featuring a fluorophenyl group and an oxadiazole ring, makes it a valuable intermediate for designing potential drugs targeting neurological disorders and inflammation. Researchers explore its use in creating compounds with enhanced binding affinity to specific receptors or enzymes, which could lead to the development of new therapeutic agents. Additionally, it serves as a key building block in medicinal chemistry for optimizing drug candidates with improved efficacy and reduced side effects. Its application extends to the study of structure-activity relationships (SAR) to better understand how chemical modifications influence biological activity.
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