4-Bromo-N-(4-fluoro-3-(trifluoromethyl)phenyl)benzenesulfonamide
97%
- Product Code: 119381
CAS:
1022050-36-7
Molecular Weight: | 398.17 g./mol | Molecular Formula: | C₁₃H₈BrF₄NO₂S |
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EC Number: | MDL Number: | MFCD13891235 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | Room temperature, sealed, dry, dark |
Product Description:
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring bromo and fluoro substituents, makes it valuable for creating potential drug candidates, particularly in the development of enzyme inhibitors or receptor modulators. The trifluoromethyl group enhances its metabolic stability and lipophilicity, which is crucial for optimizing drug-like properties. It is often employed in medicinal chemistry to explore treatments for conditions such as inflammation, cancer, or neurological disorders. Additionally, its unique chemical structure allows for further functionalization, enabling researchers to tailor compounds for specific therapeutic targets.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿1,485.00 |
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0.250 | 10-20 days | ฿2,511.00 |
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1.000 | 10-20 days | ฿6,759.00 |
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4-Bromo-N-(4-fluoro-3-(trifluoromethyl)phenyl)benzenesulfonamide
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring bromo and fluoro substituents, makes it valuable for creating potential drug candidates, particularly in the development of enzyme inhibitors or receptor modulators. The trifluoromethyl group enhances its metabolic stability and lipophilicity, which is crucial for optimizing drug-like properties. It is often employed in medicinal chemistry to explore treatments for conditions such as inflammation, cancer, or neurological disorders. Additionally, its unique chemical structure allows for further functionalization, enabling researchers to tailor compounds for specific therapeutic targets.
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