4-(methylthio)benzene-1-sulfonylchloride

95%

Reagent Code: #208168
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CAS Number 1129-25-5

science Other reagents with same CAS 1129-25-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.71 g/mol
Formula C₇H₇ClO₂S₂
thermostat Physical Properties
Boiling Point 321.009ºC at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry for constructing sulfonamide-based drugs. Its sulfonyl chloride group readily reacts with amines to form sulfonamides, which are key structural motifs in many bioactive molecules, including antimicrobial and anti-inflammatory agents. The methylthio substituent can act as a directing group in electrophilic aromatic substitution or be further modified to thioethers, sulfoxides, or sulfones, expanding its utility in synthetic pathways. Also employed in the development of agrochemicals and functional materials due to its reactivity and stability as a building block.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,770.00
inventory 200mg
10-20 days ฿4,660.00
4-(methylthio)benzene-1-sulfonylchloride
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Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry for constructing sulfonamide-based drugs. Its sulfonyl chloride group readily reacts with amines to form sulfonamides, which are key structural motifs in many bioactive molecules, including antimicrobial and anti-inflammatory agents. The methylthio substituent can act as a directing group in electrophilic aromatic substitution or be further modified to thioethers, sulfoxides, or sulfones, expanding its utili

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry for constructing sulfonamide-based drugs. Its sulfonyl chloride group readily reacts with amines to form sulfonamides, which are key structural motifs in many bioactive molecules, including antimicrobial and anti-inflammatory agents. The methylthio substituent can act as a directing group in electrophilic aromatic substitution or be further modified to thioethers, sulfoxides, or sulfones, expanding its utility in synthetic pathways. Also employed in the development of agrochemicals and functional materials due to its reactivity and stability as a building block.

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