4-Ethenylbenzenesulfonyl Chloride

95%, stabilized with TBC

Reagent Code: #182158
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CAS Number 2633-67-2

science Other reagents with same CAS 2633-67-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.66 g/mol
Formula C₈H₇ClO₂S
badge Registry Numbers
MDL Number MFCD00080678
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as a reactive intermediate in organic synthesis, this compound serves as a sulfonyl chloride building block for introducing sulfone functionalities into target molecules. Its vinyl group allows for further functionalization through reactions such as cross-coupling or polymerization, making it valuable in the development of pharmaceuticals, agrochemicals, and specialty polymers. It is also employed in the preparation of sulfonate esters and sulfonamides, which are common motifs in bioactive compounds. Due to its reactivity, it is handled under controlled conditions for safe and efficient use in research and industrial applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,160.00
inventory 250mg
10-20 days ฿5,390.00
inventory 5g
10-20 days ฿69,360.00
inventory 1g
10-20 days ฿14,490.00
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4-Ethenylbenzenesulfonyl Chloride
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Used primarily as a reactive intermediate in organic synthesis, this compound serves as a sulfonyl chloride building block for introducing sulfone functionalities into target molecules. Its vinyl group allows for further functionalization through reactions such as cross-coupling or polymerization, making it valuable in the development of pharmaceuticals, agrochemicals, and specialty polymers. It is also employed in the preparation of sulfonate esters and sulfonamides, which are common motifs in bioactive

Used primarily as a reactive intermediate in organic synthesis, this compound serves as a sulfonyl chloride building block for introducing sulfone functionalities into target molecules. Its vinyl group allows for further functionalization through reactions such as cross-coupling or polymerization, making it valuable in the development of pharmaceuticals, agrochemicals, and specialty polymers. It is also employed in the preparation of sulfonate esters and sulfonamides, which are common motifs in bioactive compounds. Due to its reactivity, it is handled under controlled conditions for safe and efficient use in research and industrial applications.

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