4-bromo-N,N-diethyl-2-fluorobenzenesulfonamide
95%
- Product Code: 46666
CAS:
1055995-87-3
| Molecular Weight: | 310.1831232 g./mol | Molecular Formula: | C₁₀H₁₃BrFNO₂S |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex chemical structures. Its unique combination of bromo, fluoro, and sulfonamide groups makes it valuable in pharmaceutical research, particularly in the design of drug candidates with specific biological activities. The presence of the sulfonamide group allows it to interact with enzymes or receptors, making it useful in the study of enzyme inhibition or receptor modulation. Additionally, the bromo and fluoro substituents provide reactive sites for further functionalization, enabling the creation of diverse derivatives for material science applications or as building blocks in medicinal chemistry. Its role in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, is also noteworthy, as it facilitates the formation of carbon-carbon or carbon-nitrogen bonds in the synthesis of advanced organic compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $2,158.47 |
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4-bromo-N,N-diethyl-2-fluorobenzenesulfonamide
This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex chemical structures. Its unique combination of bromo, fluoro, and sulfonamide groups makes it valuable in pharmaceutical research, particularly in the design of drug candidates with specific biological activities. The presence of the sulfonamide group allows it to interact with enzymes or receptors, making it useful in the study of enzyme inhibition or receptor modulation. Additionally, the bromo and fluoro substituents provide reactive sites for further functionalization, enabling the creation of diverse derivatives for material science applications or as building blocks in medicinal chemistry. Its role in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, is also noteworthy, as it facilitates the formation of carbon-carbon or carbon-nitrogen bonds in the synthesis of advanced organic compounds.
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