N-(3-Bromo-4-fluorophenyl)methanesulfonamide
≥97%
- Product Code: 69583
CAS:
1256633-26-7
| Molecular Weight: | 268.10 g./mol | Molecular Formula: | C₇H₇BrFNO₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18071053 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a valuable intermediate for the development of more complex chemical structures. It is particularly useful in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs) that target specific biological pathways. The presence of both bromo and fluoro substituents on the aromatic ring makes it a versatile building block for the introduction of these halogens into target molecules, which can significantly alter the biological activity and metabolic stability of the resulting compounds. Additionally, it is employed in the research and development of new drugs, especially in the area of kinase inhibitors, where such halogenated aromatic systems are often key components. Its application extends to material science as well, where it can be used to modify the properties of polymers and other materials through chemical reactions that involve the sulfonamide group.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,557.00 |
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| 5.000 | 10-20 days | ฿6,318.00 |
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N-(3-Bromo-4-fluorophenyl)methanesulfonamide
This compound is primarily utilized in the field of organic synthesis, where it serves as a valuable intermediate for the development of more complex chemical structures. It is particularly useful in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs) that target specific biological pathways. The presence of both bromo and fluoro substituents on the aromatic ring makes it a versatile building block for the introduction of these halogens into target molecules, which can significantly alter the biological activity and metabolic stability of the resulting compounds. Additionally, it is employed in the research and development of new drugs, especially in the area of kinase inhibitors, where such halogenated aromatic systems are often key components. Its application extends to material science as well, where it can be used to modify the properties of polymers and other materials through chemical reactions that involve the sulfonamide group.
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