3-BROMO-2-CHLOROBENZENESULFONYL CHLORIDE

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Reagent Code: #156339
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CAS Number 100191-17-1

science Other reagents with same CAS 100191-17-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 289.96 g/mol
Formula C₆H₃BrCl₂O₂S
badge Registry Numbers
MDL Number MFCD18379734
thermostat Physical Properties
Boiling Point 353.8±32.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.880±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactive sulfonyl chloride group enables the formation of sulfonamides, which are key structural motifs in many biologically active compounds. Commonly employed in the development of herbicides and fungicides due to the enhanced stability and lipophilicity imparted by the halogenated aromatic ring. Also utilized in the preparation of dyes and functional polymers where sulfonyl chloride groups act as cross-linking or chain-extension agents. Its halogen substituents allow for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿18,980.00

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3-BROMO-2-CHLOROBENZENESULFONYL CHLORIDE
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactive sulfonyl chloride group enables the formation of sulfonamides, which are key structural motifs in many biologically active compounds. Commonly employed in the development of herbicides and fungicides due to the enhanced stability and lipophilicity imparted by the halogenated aromatic ring. Also utilized in the preparation of dyes and functional polymers where sulfonyl chloride groups act as cross-linking

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactive sulfonyl chloride group enables the formation of sulfonamides, which are key structural motifs in many biologically active compounds. Commonly employed in the development of herbicides and fungicides due to the enhanced stability and lipophilicity imparted by the halogenated aromatic ring. Also utilized in the preparation of dyes and functional polymers where sulfonyl chloride groups act as cross-linking or chain-extension agents. Its halogen substituents allow for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules.

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