5-Methyl-2-nitrobenzene-1-sulfonylchloride

98%

Reagent Code: #213501
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CAS Number 173908-60-6

science Other reagents with same CAS 173908-60-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 235.64 g/mol
Formula C₇H₆ClNO₄S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. It serves as a sulfonylating agent to introduce the 5-methyl-2-nitrobenzenesulfonyl group into molecules, aiding in the protection of amines or modification of reactivity during multi-step syntheses. Its electron-withdrawing nitro group enhances the electrophilicity of the sulfonyl chloride, making it effective in forming sulfonamides, which are key structural motifs in certain bioactive compounds. Also employed in the development of dyes and functional materials where nitroaromatics contribute to desired electronic or optical properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,090.00
inventory 250mg
10-20 days ฿18,850.00
inventory 1g
10-20 days ฿50,860.00
5-Methyl-2-nitrobenzene-1-sulfonylchloride
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Used primarily as an intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. It serves as a sulfonylating agent to introduce the 5-methyl-2-nitrobenzenesulfonyl group into molecules, aiding in the protection of amines or modification of reactivity during multi-step syntheses. Its electron-withdrawing nitro group enhances the electrophilicity of the sulfonyl chloride, making it effective in forming sulfonamides, which are key structural motifs in certain bioactiv

Used primarily as an intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. It serves as a sulfonylating agent to introduce the 5-methyl-2-nitrobenzenesulfonyl group into molecules, aiding in the protection of amines or modification of reactivity during multi-step syntheses. Its electron-withdrawing nitro group enhances the electrophilicity of the sulfonyl chloride, making it effective in forming sulfonamides, which are key structural motifs in certain bioactive compounds. Also employed in the development of dyes and functional materials where nitroaromatics contribute to desired electronic or optical properties.

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