3-(Chlorosulfonyl)-5-fluorobenzoic acid

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Reagent Code: #165847
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CAS Number 912577-43-6

science Other reagents with same CAS 912577-43-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 238.62 g/mol
Formula C₇H₄ClFO₄S
badge Registry Numbers
MDL Number MFCD09040949
thermostat Physical Properties
Boiling Point 390.2±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.670±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used primarily as an intermediate in the synthesis of sulfa drugs and other fluorinated pharmaceutical compounds. Its reactive chlorosulfonyl group allows for easy attachment to amines, forming sulfonamide linkages common in antimicrobial agents. Also employed in the preparation of agrochemicals and dyes where fluorinated aromatic structures enhance stability and bioactivity. Commonly used in research settings to introduce fluorinated benzoic acid moieties into larger molecules for drug discovery and development.

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inventory 1g
10-20 days ฿28,360.00

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3-(Chlorosulfonyl)-5-fluorobenzoic acid
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Used primarily as an intermediate in the synthesis of sulfa drugs and other fluorinated pharmaceutical compounds. Its reactive chlorosulfonyl group allows for easy attachment to amines, forming sulfonamide linkages common in antimicrobial agents. Also employed in the preparation of agrochemicals and dyes where fluorinated aromatic structures enhance stability and bioactivity. Commonly used in research settings to introduce fluorinated benzoic acid moieties into larger molecules for drug discovery and dev

Used primarily as an intermediate in the synthesis of sulfa drugs and other fluorinated pharmaceutical compounds. Its reactive chlorosulfonyl group allows for easy attachment to amines, forming sulfonamide linkages common in antimicrobial agents. Also employed in the preparation of agrochemicals and dyes where fluorinated aromatic structures enhance stability and bioactivity. Commonly used in research settings to introduce fluorinated benzoic acid moieties into larger molecules for drug discovery and development.

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