4-Fluoro-N-(4H-1,2,4-triazol-4-yl)benzamide
90%
- Product Code: 46891
CAS:
331434-05-0
| Molecular Weight: | 206.1765 g./mol | Molecular Formula: | C₉H₇FN₄O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00448017 | |
| Melting Point: | Boiling Point: | ||
| Density: | 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 fluorinated benzamide moiety, makes it a valuable building block for developing potential pharmaceutical agents. It is often explored in the design of compounds targeting enzymes or receptors, particularly in the development of antifungal, antibacterial, or anticancer drugs. The presence of the fluorine atom enhances the compound's metabolic stability and binding affinity, making it a promising candidate for drug discovery and optimization studies. Additionally, it may be used in research to study structure-activity relationships (SAR) to improve the efficacy and selectivity of therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,627.00 |
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4-Fluoro-N-(4H-1,2,4-triazol-4-yl)benzamide
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 fluorinated benzamide moiety, makes it a valuable building block for developing potential pharmaceutical agents. It is often explored in the design of compounds targeting enzymes or receptors, particularly in the development of antifungal, antibacterial, or anticancer drugs. The presence of the fluorine atom enhances the compound's metabolic stability and binding affinity, making it a promising candidate for drug discovery and optimization studies. Additionally, it may be used in research to study structure-activity relationships (SAR) to improve the efficacy and selectivity of therapeutic agents.
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