5-Chlorothiophene-2-sulfonyl fluoride

95%

Reagent Code: #129267
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CAS Number 108158-05-0

science Other reagents with same CAS 108158-05-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.64 g/mol
Formula C₄H₂ClFO₂S₂
thermostat Physical Properties
Boiling Point 250.5±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.571 g/cm3 at 25 °C
Storage Room temperature, seal, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of sulfonamide-based drugs. Its sulfonyl fluoride group enables selective reactions with nucleophiles, making it valuable in medicinal chemistry for building bioactive molecules. Also employed in agrochemical synthesis to create herbicides and pesticides due to its stability and reactivity. Increasingly applied in chemical biology for probe and inhibitor design, where it acts as a warhead in covalent targeting of enzymes. Its chlorine and thiophene moieties enhance binding selectivity in drug candidates.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿6,590.00
inventory 5g
10-20 days ฿23,090.00

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5-Chlorothiophene-2-sulfonyl fluoride
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of sulfonamide-based drugs. Its sulfonyl fluoride group enables selective reactions with nucleophiles, making it valuable in medicinal chemistry for building bioactive molecules. Also employed in agrochemical synthesis to create herbicides and pesticides due to its stability and reactivity. Increasingly applied in chemical biology for probe and inhibitor design, where it acts as a warhead in covalent targeting

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of sulfonamide-based drugs. Its sulfonyl fluoride group enables selective reactions with nucleophiles, making it valuable in medicinal chemistry for building bioactive molecules. Also employed in agrochemical synthesis to create herbicides and pesticides due to its stability and reactivity. Increasingly applied in chemical biology for probe and inhibitor design, where it acts as a warhead in covalent targeting of enzymes. Its chlorine and thiophene moieties enhance binding selectivity in drug candidates.

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