2,2-Difluoroethenyl 4-methylbenzene-1-sulfonate

95%

Reagent Code: #178449
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CAS Number 185739-14-4

science Other reagents with same CAS 185739-14-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.22 g/mol
Formula C₉H₈F₂O₃S
badge Registry Numbers
MDL Number MFCD27946567
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. Its structure allows for selective introduction of fluorinated vinyl groups, which can enhance metabolic stability and bioavailability in active compounds. Commonly employed in cross-coupling reactions and sulfonate displacement reactions to form carbon-carbon or carbon-heteroatom bonds. Valuable in the preparation of fluorinated analogs in medicinal chemistry due to the unique electronic and steric properties imparted by the difluoroethenyl group.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,100.00
inventory 250mg
10-20 days ฿1,850.00
inventory 1g
10-20 days ฿5,320.00
inventory 5g
10-20 days ฿20,870.00

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2,2-Difluoroethenyl 4-methylbenzene-1-sulfonate
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Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. Its structure allows for selective introduction of fluorinated vinyl groups, which can enhance metabolic stability and bioavailability in active compounds. Commonly employed in cross-coupling reactions and sulfonate displacement reactions to form carbon-carbon or carbon-heteroatom bonds. Valuable in the preparation of fluorinated analogs in medicinal chemistry due to the unique elec

Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. Its structure allows for selective introduction of fluorinated vinyl groups, which can enhance metabolic stability and bioavailability in active compounds. Commonly employed in cross-coupling reactions and sulfonate displacement reactions to form carbon-carbon or carbon-heteroatom bonds. Valuable in the preparation of fluorinated analogs in medicinal chemistry due to the unique electronic and steric properties imparted by the difluoroethenyl group.

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