4-Bromo-N-(2-Methyl-3-Nitrophenyl)Benzenesulfonamide

98%

Reagent Code: #154004
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CAS Number 349085-59-2

science Other reagents with same CAS 349085-59-2

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Weight 371.21 g/mol
Formula C₁₃H₁₁BrN₂O₄S
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of sulfonamide-based pharmaceuticals. It serves as a key building block in medicinal chemistry for creating potential antimicrobial, anti-inflammatory, and anticancer agents. The presence of bromo and nitro groups allows for further functionalization through cross-coupling reactions and nucleophilic substitutions, making it valuable in drug discovery and optimization. Also employed in research settings to design enzyme inhibitors and explore structure-activity relationships in sulfonamide derivatives.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,370.00

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4-Bromo-N-(2-Methyl-3-Nitrophenyl)Benzenesulfonamide
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Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of sulfonamide-based pharmaceuticals. It serves as a key building block in medicinal chemistry for creating potential antimicrobial, anti-inflammatory, and anticancer agents. The presence of bromo and nitro groups allows for further functionalization through cross-coupling reactions and nucleophilic substitutions, making it valuable in drug discovery and optimization. Also employed in research setti

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of sulfonamide-based pharmaceuticals. It serves as a key building block in medicinal chemistry for creating potential antimicrobial, anti-inflammatory, and anticancer agents. The presence of bromo and nitro groups allows for further functionalization through cross-coupling reactions and nucleophilic substitutions, making it valuable in drug discovery and optimization. Also employed in research settings to design enzyme inhibitors and explore structure-activity relationships in sulfonamide derivatives.

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