4-Nitrobenzenesulfonamide

98%

Reagent Code: #216812
label
Alias p-nitrobenzenesulfonamide
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CAS Number 6325-93-5

science Other reagents with same CAS 6325-93-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.19 g/mol
Formula C₆H₆N₂O₄S
badge Registry Numbers
EC Number 228-691-6
MDL Number MFCD00007937
thermostat Physical Properties
Melting Point 178-180 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of sulfonamide-based pharmaceuticals. It serves as a building block for bioactive molecules, including antimicrobial and antiviral agents. Its nitro group allows for further functionalization through reduction to an amine, enabling the formation of more complex sulfonamide derivatives. Also employed in the development of dyes and fluorescent probes due to its electron-withdrawing properties and stability. In research, it acts as a reagent for modifying amines in peptide chemistry through sulfonylation reactions.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿300.00
inventory 25g
10-20 days ฿1,300.00
inventory 100g
10-20 days ฿4,990.00

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4-Nitrobenzenesulfonamide
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Used as an intermediate in organic synthesis, particularly in the preparation of sulfonamide-based pharmaceuticals. It serves as a building block for bioactive molecules, including antimicrobial and antiviral agents. Its nitro group allows for further functionalization through reduction to an amine, enabling the formation of more complex sulfonamide derivatives. Also employed in the development of dyes and fluorescent probes due to its electron-withdrawing properties and stability. In research, it acts a

Used as an intermediate in organic synthesis, particularly in the preparation of sulfonamide-based pharmaceuticals. It serves as a building block for bioactive molecules, including antimicrobial and antiviral agents. Its nitro group allows for further functionalization through reduction to an amine, enabling the formation of more complex sulfonamide derivatives. Also employed in the development of dyes and fluorescent probes due to its electron-withdrawing properties and stability. In research, it acts as a reagent for modifying amines in peptide chemistry through sulfonylation reactions.

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