N-(2-Amino-4-fluorophenyl)methanesulfonamide
98%
- Product Code: 50149
CAS:
156522-13-3
| Molecular Weight: | 204.2220 g./mol | Molecular Formula: | C₇H₉FN₂O₂S |
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| EC Number: | MDL Number: | MFCD09047153 | |
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| 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 both an amino group and a sulfonamide moiety, makes it a valuable building block for developing potential therapeutic agents. Specifically, it has been explored in the design and synthesis of novel compounds targeting enzyme inhibition, particularly in the context of anti-inflammatory and anticancer drug development. The fluorine atom in its structure enhances its binding affinity to target proteins, improving the efficacy of the resulting drugs. Additionally, it has been investigated for its role in creating fluorescent probes used in biochemical research to study enzyme activity and protein interactions. Its versatility and functional groups make it a significant compound in drug discovery and biochemical studies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿3,825.00 |
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N-(2-Amino-4-fluorophenyl)methanesulfonamide
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 both an amino group and a sulfonamide moiety, makes it a valuable building block for developing potential therapeutic agents. Specifically, it has been explored in the design and synthesis of novel compounds targeting enzyme inhibition, particularly in the context of anti-inflammatory and anticancer drug development. The fluorine atom in its structure enhances its binding affinity to target proteins, improving the efficacy of the resulting drugs. Additionally, it has been investigated for its role in creating fluorescent probes used in biochemical research to study enzyme activity and protein interactions. Its versatility and functional groups make it a significant compound in drug discovery and biochemical studies.
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