4-(4-chlorophenyl)benzenesulfonyl chloride

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Reagent Code: #162633
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CAS Number 20443-74-7

science Other reagents with same CAS 20443-74-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 287.17 g/mol
Formula C₁₂H₈Cl₂O₂S
badge Registry Numbers
MDL Number MFCD01631918
thermostat Physical Properties
Melting Point 108-110 °C
Boiling Point 400.8 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.412 g/cm3
Storage Room temperature

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves as a building block in the preparation of sulfonamide derivatives, which are important in the development of antimicrobial and anti-inflammatory agents. Its reactivity allows for easy introduction of the 4-(4-chlorophenyl)phenylsulfonyl group into target molecules, enhancing structural diversity in drug discovery. Also employed in the production of dyes and functional materials where sulfonyl chloride groups enable covalent attachment to other molecular frameworks.

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Test Parameter Specification
Appearance White to Yellow Powder
Purity (%) 96.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,890.00
inventory 1g
10-20 days ฿5,540.00
inventory 5g
10-20 days ฿12,282.00

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4-(4-chlorophenyl)benzenesulfonyl chloride
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves as a building block in the preparation of sulfonamide derivatives, which are important in the development of antimicrobial and anti-inflammatory agents. Its reactivity allows for easy introduction of the 4-(4-chlorophenyl)phenylsulfonyl group into target molecules, enhancing structural diversity in drug discovery. Also employed in the production of dyes and functional materials where sulfonyl chloride group

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves as a building block in the preparation of sulfonamide derivatives, which are important in the development of antimicrobial and anti-inflammatory agents. Its reactivity allows for easy introduction of the 4-(4-chlorophenyl)phenylsulfonyl group into target molecules, enhancing structural diversity in drug discovery. Also employed in the production of dyes and functional materials where sulfonyl chloride groups enable covalent attachment to other molecular frameworks.

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