Ethyl Phenyl Sulfone

97%

Reagent Code: #182182
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CAS Number 599-70-2

science Other reagents with same CAS 599-70-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 170.23 g/mol
Formula C₈H₁₀O₂S
badge Registry Numbers
MDL Number MFCD00025081
thermostat Physical Properties
Melting Point 35-40°C (Lit.)
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical manufacturing. It serves as a building block in the production of sulfone-based compounds with biological activity. Commonly employed in cross-coupling reactions due to the stability of the sulfone group, enabling the formation of carbon-carbon bonds. Also utilized in the development of functional materials and as a reagent in research laboratories for modifying molecular structures. Its electron-withdrawing nature makes it valuable in directed ortho-metalation processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿990.00
inventory 5g
10-20 days ฿3,190.00
inventory 100g
10-20 days ฿26,980.00
inventory 25g
10-20 days ฿10,750.00
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Ethyl Phenyl Sulfone
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Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical manufacturing. It serves as a building block in the production of sulfone-based compounds with biological activity. Commonly employed in cross-coupling reactions due to the stability of the sulfone group, enabling the formation of carbon-carbon bonds. Also utilized in the development of functional materials and as a reagent in research laboratories for modifying molecular structures. Its electron-withdrawing nat

Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical manufacturing. It serves as a building block in the production of sulfone-based compounds with biological activity. Commonly employed in cross-coupling reactions due to the stability of the sulfone group, enabling the formation of carbon-carbon bonds. Also utilized in the development of functional materials and as a reagent in research laboratories for modifying molecular structures. Its electron-withdrawing nature makes it valuable in directed ortho-metalation processes.

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