4-Methyl-2-nitrobenzene-1-sulfonyl chloride

95%

Reagent Code: #203369
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CAS Number 54090-41-4

science Other reagents with same CAS 54090-41-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 235.64 g/mol
Formula C₇H₆NO₄SCl
badge Registry Numbers
MDL Number MFCD01365819
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used primarily as a chemical intermediate in organic synthesis, particularly in the preparation of dyes, pharmaceuticals, and agrochemicals. Its sulfonyl chloride group readily reacts with amines to form sulfonamides, which are key structural motifs in many biologically active compounds. It also serves as a derivatizing agent in analytical chemistry for the detection and quantification of amine-containing substances. Due to the electron-withdrawing nitro group and the methyl substituent, it offers selective reactivity useful in multi-step synthesis where controlled functionalization is required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,140.00
inventory 250mg
10-20 days ฿7,030.00
inventory 1g
10-20 days ฿18,980.00
4-Methyl-2-nitrobenzene-1-sulfonyl chloride
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Used primarily as a chemical intermediate in organic synthesis, particularly in the preparation of dyes, pharmaceuticals, and agrochemicals. Its sulfonyl chloride group readily reacts with amines to form sulfonamides, which are key structural motifs in many biologically active compounds. It also serves as a derivatizing agent in analytical chemistry for the detection and quantification of amine-containing substances. Due to the electron-withdrawing nitro group and the methyl substituent, it offers select

Used primarily as a chemical intermediate in organic synthesis, particularly in the preparation of dyes, pharmaceuticals, and agrochemicals. Its sulfonyl chloride group readily reacts with amines to form sulfonamides, which are key structural motifs in many biologically active compounds. It also serves as a derivatizing agent in analytical chemistry for the detection and quantification of amine-containing substances. Due to the electron-withdrawing nitro group and the methyl substituent, it offers selective reactivity useful in multi-step synthesis where controlled functionalization is required.

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