5-(4-Fluorophenyl)-4-methyl-4H-1,2,4-triazole-3-thiol
95%
- Product Code: 48236
CAS:
138417-35-3
| Molecular Weight: | 209.2433 g./mol | Molecular Formula: | C₉H₈FN₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01940414 | |
| Melting Point: | Boiling Point: | 266.3 °C at 760 mmHg | |
| Density: | 1.38g/cm3 | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a triazole ring and a fluorophenyl group, makes it a valuable building block for developing compounds with potential therapeutic properties. It is often explored in the design of antifungal, antibacterial, and antiviral agents due to its ability to interact with biological targets effectively. Additionally, its thiol group allows for further functionalization, enabling the creation of derivatives with enhanced pharmacological activities. Researchers also investigate its role in developing enzyme inhibitors, particularly those targeting enzymes involved in disease pathways. Its versatility and reactivity make it a significant compound in drug discovery and development processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,177.00 |
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5-(4-Fluorophenyl)-4-methyl-4H-1,2,4-triazole-3-thiol
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a triazole ring and a fluorophenyl group, makes it a valuable building block for developing compounds with potential therapeutic properties. It is often explored in the design of antifungal, antibacterial, and antiviral agents due to its ability to interact with biological targets effectively. Additionally, its thiol group allows for further functionalization, enabling the creation of derivatives with enhanced pharmacological activities. Researchers also investigate its role in developing enzyme inhibitors, particularly those targeting enzymes involved in disease pathways. Its versatility and reactivity make it a significant compound in drug discovery and development processes.
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