methyl5-(chlorosulfonyl)furan-3-carboxylate

95%

Reagent Code: #213200
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CAS Number 1306607-16-8

science Other reagents with same CAS 1306607-16-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224.62 g/mol
Formula C₆H₅ClO₅S
badge Registry Numbers
MDL Number MFCD18839058
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactive chlorosulfonyl group allows for easy modification to sulfonamide or sulfonic acid derivatives, which are common motifs in bioactive molecules. It is particularly valuable in the development of herbicides and fungicides due to the enhanced stability and membrane permeability provided by the furan ring. Also employed in the preparation of specialty polymers and functional materials where sulfonyl-containing esters act as crosslinking agents or catalysts. Its ester functionality enables further chain extension or coupling reactions, making it useful in combinatorial chemistry and drug discovery.

Available Sizes & Pricing

Size Availability Unit Price Quantity
50mg
10-20 days ฿5,880.00
methyl5-(chlorosulfonyl)furan-3-carboxylate
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactive chlorosulfonyl group allows for easy modification to sulfonamide or sulfonic acid derivatives, which are common motifs in bioactive molecules. It is particularly valuable in the development of herbicides and fungicides due to the enhanced stability and membrane permeability provided by the furan ring. Also employed in the preparation of specialty polymers and functional materials where sulfonyl-containin

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactive chlorosulfonyl group allows for easy modification to sulfonamide or sulfonic acid derivatives, which are common motifs in bioactive molecules. It is particularly valuable in the development of herbicides and fungicides due to the enhanced stability and membrane permeability provided by the furan ring. Also employed in the preparation of specialty polymers and functional materials where sulfonyl-containing esters act as crosslinking agents or catalysts. Its ester functionality enables further chain extension or coupling reactions, making it useful in combinatorial chemistry and drug discovery.

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