N-(3-Bromophenyl)benzenesulfonamide

95%

Reagent Code: #219470
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CAS Number 91394-73-9

science Other reagents with same CAS 91394-73-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 312.18 g/mol
Formula C₁₂H₁₀BrNO₂S
badge Registry Numbers
MDL Number MFCD01030655
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure allows for further functionalization through cross-coupling reactions, making it valuable in the preparation of bioactive molecules. Commonly employed in the synthesis of sulfonamide-based compounds that exhibit antimicrobial or anti-inflammatory properties. Also utilized in research settings for the design of novel enzyme inhibitors due to the sulfonamide group's ability to interact with biological targets.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,490.00
inventory 250mg
10-20 days ฿2,230.00
inventory 1g
10-20 days ฿5,570.00

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N-(3-Bromophenyl)benzenesulfonamide
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Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure allows for further functionalization through cross-coupling reactions, making it valuable in the preparation of bioactive molecules. Commonly employed in the synthesis of sulfonamide-based compounds that exhibit antimicrobial or anti-inflammatory properties. Also utilized in research settings for the design of novel enzyme inhibitors due to the sulfonamide group's ability to inte
Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure allows for further functionalization through cross-coupling reactions, making it valuable in the preparation of bioactive molecules. Commonly employed in the synthesis of sulfonamide-based compounds that exhibit antimicrobial or anti-inflammatory properties. Also utilized in research settings for the design of novel enzyme inhibitors due to the sulfonamide group's ability to interact with biological targets.
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