4-Ethylbenzenesulfonyl chloride

95%,GC

Reagent Code: #182852
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CAS Number 16712-69-9

science Other reagents with same CAS 16712-69-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.68 g/mol
Formula C₈H₉ClO₂S
badge Registry Numbers
MDL Number MFCD00041480
thermostat Physical Properties
Melting Point 8-12°C
Boiling Point 134°C
inventory_2 Storage & Handling
Density 1.268 g/cm3
Storage Room temperature, inert gas environment

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of sulfonamides, which are important in pharmaceuticals and agrochemicals. It reacts with amines to form sulfonamide derivatives, commonly found in drugs with antimicrobial, anti-inflammatory, and antidiabetic properties. Also employed in the development of dyes and polymers due to its reactivity and ability to introduce sulfonyl functional groups. Its ethyl-substituted aromatic ring enhances lipophilicity, making it useful in modifying drug molecules for improved membrane permeability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿450.00
inventory 5g
10-20 days ฿1,400.00
inventory 25g
10-20 days ฿4,850.00
inventory 100g
10-20 days ฿17,380.00
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4-Ethylbenzenesulfonyl chloride
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Used as an intermediate in organic synthesis, particularly in the preparation of sulfonamides, which are important in pharmaceuticals and agrochemicals. It reacts with amines to form sulfonamide derivatives, commonly found in drugs with antimicrobial, anti-inflammatory, and antidiabetic properties. Also employed in the development of dyes and polymers due to its reactivity and ability to introduce sulfonyl functional groups. Its ethyl-substituted aromatic ring enhances lipophilicity, making it useful in

Used as an intermediate in organic synthesis, particularly in the preparation of sulfonamides, which are important in pharmaceuticals and agrochemicals. It reacts with amines to form sulfonamide derivatives, commonly found in drugs with antimicrobial, anti-inflammatory, and antidiabetic properties. Also employed in the development of dyes and polymers due to its reactivity and ability to introduce sulfonyl functional groups. Its ethyl-substituted aromatic ring enhances lipophilicity, making it useful in modifying drug molecules for improved membrane permeability.

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