4-bromo-N,N-diethyl-2-fluorobenzenesulfonamide

95%

Reagent Code: #46666
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CAS Number 1055995-87-3

science Other reagents with same CAS 1055995-87-3

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Weight 310.1831232 g/mol
Formula C₁₀H₁₃BrFNO₂S
inventory_2 Storage & Handling
Storage 2-8°C

description 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.

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inventory 100mg
10-20 days ฿51,975.00

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4-bromo-N,N-diethyl-2-fluorobenzenesulfonamide
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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

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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