2,3-Dichlorobenzenesulfonyl Chloride

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Reagent Code: #170863
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CAS Number 82417-45-6

science Other reagents with same CAS 82417-45-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.51 g/mol
Formula C₆H₃Cl₃O₂S
badge Registry Numbers
MDL Number MFCD00051844
thermostat Physical Properties
Melting Point 60-64°C (Lit.)
inventory_2 Storage & Handling
Storage 2-8℃, dry

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It plays a key role in the preparation of sulfa drugs and herbicides due to its ability to introduce sulfonyl functional groups into organic molecules. Its reactivity makes it valuable in forming sulfonamides, which are important in antimicrobial agents. Also utilized in the development of dyes and pigments for enhanced color stability. Common in research settings for constructing complex molecules requiring selective chlorination and sulfonylation.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿590.00
inventory 25g
10-20 days ฿1,419.00

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2,3-Dichlorobenzenesulfonyl Chloride
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It plays a key role in the preparation of sulfa drugs and herbicides due to its ability to introduce sulfonyl functional groups into organic molecules. Its reactivity makes it valuable in forming sulfonamides, which are important in antimicrobial agents. Also utilized in the development of dyes and pigments for enhanced color stability. Common in research settings for constructing complex molecules requiring selectiv

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It plays a key role in the preparation of sulfa drugs and herbicides due to its ability to introduce sulfonyl functional groups into organic molecules. Its reactivity makes it valuable in forming sulfonamides, which are important in antimicrobial agents. Also utilized in the development of dyes and pigments for enhanced color stability. Common in research settings for constructing complex molecules requiring selective chlorination and sulfonylation.

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