2,4-Dinitrobenzenesulfonyl chloride

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Reagent Code: #170321
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CAS Number 1656-44-6

science Other reagents with same CAS 1656-44-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 266.62 g/mol
Formula C₆H₃ClN₂O₆S
badge Registry Numbers
MDL Number MFCD00007431
thermostat Physical Properties
Melting Point 100-104°C
inventory_2 Storage & Handling
Storage 2-8°C, Inert gas protection

description Product Description

Widely used in organic synthesis as a derivatizing agent for amines and other nucleophiles. It introduces the 2,4-dinitrobenzenesulfonyl (DNBS) group, which enhances the detectability and stability of compounds in analytical methods. Commonly applied in the preparation of sulfonamides for pharmaceutical research. Also serves as an intermediate in the development of dyes, agrochemicals, and specialty polymers. Its strong electron-withdrawing nature makes it useful in modifying reactivity in multi-step synthesis.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,410.00
inventory 5g
10-20 days ฿7,000.00
inventory 25g
10-20 days ฿23,990.00

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2,4-Dinitrobenzenesulfonyl chloride
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Widely used in organic synthesis as a derivatizing agent for amines and other nucleophiles. It introduces the 2,4-dinitrobenzenesulfonyl (DNBS) group, which enhances the detectability and stability of compounds in analytical methods. Commonly applied in the preparation of sulfonamides for pharmaceutical research. Also serves as an intermediate in the development of dyes, agrochemicals, and specialty polymers. Its strong electron-withdrawing nature makes it useful in modifying reactivity in multi-step syn

Widely used in organic synthesis as a derivatizing agent for amines and other nucleophiles. It introduces the 2,4-dinitrobenzenesulfonyl (DNBS) group, which enhances the detectability and stability of compounds in analytical methods. Commonly applied in the preparation of sulfonamides for pharmaceutical research. Also serves as an intermediate in the development of dyes, agrochemicals, and specialty polymers. Its strong electron-withdrawing nature makes it useful in modifying reactivity in multi-step synthesis.

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