2-(Chlorosulfonyl)benzoic acid

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Reagent Code: #161876
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CAS Number 63914-81-8

science Other reagents with same CAS 63914-81-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.63 g/mol
Formula C₇H₅ClO₄S
badge Registry Numbers
MDL Number MFCD06208087
thermostat Physical Properties
Boiling Point 384°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used primarily as an intermediate in the synthesis of sulfa drugs and other pharmaceuticals. It plays a key role in the preparation of saccharin, an artificial sweetener, by serving as a precursor in the chlorosulfonation process. Also utilized in the production of dyes and agrochemicals due to its ability to introduce sulfonyl chloride functional groups into organic molecules. Its reactivity makes it valuable in forming sulfonamide derivatives, which are common structural elements in many biologically active compounds.

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Test Parameter Specification
Appearance White to Yellow Solid
Purity (%) 89.5-100
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,250.00
inventory 250mg
10-20 days ฿11,660.00
inventory 1g
10-20 days ฿32,670.00

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2-(Chlorosulfonyl)benzoic acid
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Used primarily as an intermediate in the synthesis of sulfa drugs and other pharmaceuticals. It plays a key role in the preparation of saccharin, an artificial sweetener, by serving as a precursor in the chlorosulfonation process. Also utilized in the production of dyes and agrochemicals due to its ability to introduce sulfonyl chloride functional groups into organic molecules. Its reactivity makes it valuable in forming sulfonamide derivatives, which are common structural elements in many biologically a

Used primarily as an intermediate in the synthesis of sulfa drugs and other pharmaceuticals. It plays a key role in the preparation of saccharin, an artificial sweetener, by serving as a precursor in the chlorosulfonation process. Also utilized in the production of dyes and agrochemicals due to its ability to introduce sulfonyl chloride functional groups into organic molecules. Its reactivity makes it valuable in forming sulfonamide derivatives, which are common structural elements in many biologically active compounds.

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