3-Chloro-4-fluoro-N-[4-[[2-(phenylcarbonyl)hydrazino]carbonyl]benzyl]benzenesulfonamide
99%
- Product Code: 80323
CAS:
852918-02-6
| Molecular Weight: | 461.89 g./mol | Molecular Formula: | C₂₁H₁₇ClFN₃O₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06683895 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily used in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of biologically active molecules, particularly those targeting enzyme inhibition. Its structure suggests potential applications in the design of sulfonamide-based drugs, which are often explored for their antibacterial, anti-inflammatory, or anticancer properties. Researchers utilize this chemical to study its interactions with specific protein targets, aiding in the development of novel therapeutic agents. Additionally, its unique functional groups make it a valuable candidate for further chemical modifications to optimize pharmacological activity and selectivity.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | white to beige powder |
| PURITY | 98.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $388.54 |
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| 0.250 | 10-20 days | $843.54 |
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3-Chloro-4-fluoro-N-[4-[[2-(phenylcarbonyl)hydrazino]carbonyl]benzyl]benzenesulfonamide
This compound is primarily used in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of biologically active molecules, particularly those targeting enzyme inhibition. Its structure suggests potential applications in the design of sulfonamide-based drugs, which are often explored for their antibacterial, anti-inflammatory, or anticancer properties. Researchers utilize this chemical to study its interactions with specific protein targets, aiding in the development of novel therapeutic agents. Additionally, its unique functional groups make it a valuable candidate for further chemical modifications to optimize pharmacological activity and selectivity.
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