3-(Methylsulfonyl)benzenesulfonyl Chloride

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Reagent Code: #173664
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CAS Number 5335-40-0

science Other reagents with same CAS 5335-40-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 254.71 g/mol
Formula C₇H₇ClO₄S₂
badge Registry Numbers
MDL Number MFCD04037968
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily as a key intermediate in the synthesis of biologically active compounds, especially in pharmaceuticals and agrochemicals. Its dual functionality, featuring both sulfonyl chloride and methylsulfonyl groups, allows for sequential derivatization, making it valuable in constructing sulfonamide-based molecules. Commonly employed in the development of protease inhibitors and kinase inhibitors due to its ability to enhance binding affinity and metabolic stability. Also utilized in the preparation of fluorescent probes and functional polymers where sulfonyl groups contribute to electron-withdrawing properties and thermal stability.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿302.50
5g
10-20 days ฿1,292.50
25g
10-20 days ฿5,923.50

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3-(Methylsulfonyl)benzenesulfonyl Chloride
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Used primarily as a key intermediate in the synthesis of biologically active compounds, especially in pharmaceuticals and agrochemicals. Its dual functionality, featuring both sulfonyl chloride and methylsulfonyl groups, allows for sequential derivatization, making it valuable in constructing sulfonamide-based molecules. Commonly employed in the development of protease inhibitors and kinase inhibitors due to its ability to enhance binding affinity and metabolic stability. Also utilized in the preparation

Used primarily as a key intermediate in the synthesis of biologically active compounds, especially in pharmaceuticals and agrochemicals. Its dual functionality, featuring both sulfonyl chloride and methylsulfonyl groups, allows for sequential derivatization, making it valuable in constructing sulfonamide-based molecules. Commonly employed in the development of protease inhibitors and kinase inhibitors due to its ability to enhance binding affinity and metabolic stability. Also utilized in the preparation of fluorescent probes and functional polymers where sulfonyl groups contribute to electron-withdrawing properties and thermal stability.

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