4-Bromo-N-(3-bromophenyl)-2-fluoro-benzenesulfonamide

95%

Reagent Code: #151849
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CAS Number 1772777-01-1

science Other reagents with same CAS 1772777-01-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 409.07 g/mol
Formula C₁₂H₈Br₂FNO₂S
badge Registry Numbers
MDL Number MFCD27824753
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. It serves as a building block in the development of sulfonamide-based drugs, which exhibit anticonvulsant, anti-inflammatory, and antimicrobial properties. Its bromo and fluoro substituents allow for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry for structure-activity relationship studies. Also employed in the preparation of receptor modulators and enzyme inhibitors due to its ability to influence binding affinity and metabolic stability.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,060.00
inventory 1g
10-20 days ฿2,400.00
inventory 25g
10-20 days ฿31,280.00

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4-Bromo-N-(3-bromophenyl)-2-fluoro-benzenesulfonamide
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Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. It serves as a building block in the development of sulfonamide-based drugs, which exhibit anticonvulsant, anti-inflammatory, and antimicrobial properties. Its bromo and fluoro substituents allow for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry for structure-activity relationship studies. Also employed i

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. It serves as a building block in the development of sulfonamide-based drugs, which exhibit anticonvulsant, anti-inflammatory, and antimicrobial properties. Its bromo and fluoro substituents allow for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry for structure-activity relationship studies. Also employed in the preparation of receptor modulators and enzyme inhibitors due to its ability to influence binding affinity and metabolic stability.

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