3-Bromo-5-(fluorosulfonyl)benzoic acid

≥97%

Reagent Code: #131512
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CAS Number 2138402-24-9

science Other reagents with same CAS 2138402-24-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 283.07 g/mol
Formula C₇H₄BrFO₄S
badge Registry Numbers
MDL Number MFCD31445034
thermostat Physical Properties
Boiling Point 409.6±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.901±0.06 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its fluorosulfonyl and bromo functional groups allow for selective cross-coupling reactions, making it valuable in building complex organic molecules. Commonly employed in the development of sulfa drugs and fluorinated bioactive compounds due to its reactivity in palladium-catalyzed reactions. Also utilized in research for designing enzyme inhibitors and functional materials where precise molecular architecture is required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,000.00
inventory 250mg
10-20 days ฿14,600.00

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3-Bromo-5-(fluorosulfonyl)benzoic acid
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Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its fluorosulfonyl and bromo functional groups allow for selective cross-coupling reactions, making it valuable in building complex organic molecules. Commonly employed in the development of sulfa drugs and fluorinated bioactive compounds due to its reactivity in palladium-catalyzed reactions. Also utilized in research for designing enzyme inhibitors and functional materials where precise molecular architecture is

Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its fluorosulfonyl and bromo functional groups allow for selective cross-coupling reactions, making it valuable in building complex organic molecules. Commonly employed in the development of sulfa drugs and fluorinated bioactive compounds due to its reactivity in palladium-catalyzed reactions. Also utilized in research for designing enzyme inhibitors and functional materials where precise molecular architecture is required.

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