4-Bromo-5-(fluorosulfonyl)thiophene-2-carboxylic acid

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Reagent Code: #153014
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CAS Number 1936650-56-4

science Other reagents with same CAS 1936650-56-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 289.1 g/mol
Formula C₅H₂BrFO₄S₂
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to the presence of reactive fluorosulfonyl and carboxylic acid groups. The compound enables the construction of complex heterocyclic systems, particularly in the development of bioactive molecules where sulfur and fluorine contribute to enhanced metabolic stability and binding affinity. Its bromo and fluorosulfonyl functionalities allow for selective cross-coupling reactions and sulfonamide formation, making it valuable in medicinal chemistry for lead optimization. Also employed in materials science to design functional organic materials with tailored electronic properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,340.00
inventory 250mg
10-20 days ฿10,780.00
inventory 1g
10-20 days ฿31,510.00

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4-Bromo-5-(fluorosulfonyl)thiophene-2-carboxylic acid
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Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to the presence of reactive fluorosulfonyl and carboxylic acid groups. The compound enables the construction of complex heterocyclic systems, particularly in the development of bioactive molecules where sulfur and fluorine contribute to enhanced metabolic stability and binding affinity. Its bromo and fluorosulfonyl functionalities allow for selective cross-coupling reactions and sulfonamide formation, making

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to the presence of reactive fluorosulfonyl and carboxylic acid groups. The compound enables the construction of complex heterocyclic systems, particularly in the development of bioactive molecules where sulfur and fluorine contribute to enhanced metabolic stability and binding affinity. Its bromo and fluorosulfonyl functionalities allow for selective cross-coupling reactions and sulfonamide formation, making it valuable in medicinal chemistry for lead optimization. Also employed in materials science to design functional organic materials with tailored electronic properties.

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