4-Chloro-N-(4-hydroxynaphthalen-1-yl)-3-nitrobenzenesulfonamide

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Reagent Code: #156894
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CAS Number 420092-79-1

science Other reagents with same CAS 420092-79-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 378.79 g/mol
Formula C₁₆H₁₁ClN₂O₅S
badge Registry Numbers
MDL Number MFCD01165393
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of sulfonamide-based pharmaceuticals with potential antimicrobial and anti-inflammatory properties. Its structure allows for further functionalization, making it valuable in medicinal chemistry research for designing enzyme inhibitors. Also employed in dye synthesis due to the presence of naphthalene and nitro groups, contributing to chromophoric properties. Serves as a reagent in organic transformations where sulfonamides act as directing groups or protecting moieties.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿2,750.00
inventory 5mg
10-20 days ฿9,600.00
inventory 10mg
10-20 days ฿14,400.00

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4-Chloro-N-(4-hydroxynaphthalen-1-yl)-3-nitrobenzenesulfonamide
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Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of sulfonamide-based pharmaceuticals with potential antimicrobial and anti-inflammatory properties. Its structure allows for further functionalization, making it valuable in medicinal chemistry research for designing enzyme inhibitors. Also employed in dye synthesis due to the presence of naphthalene and nitro groups, contributing to chromophoric properties. Serves as a reagent in organic transforma

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of sulfonamide-based pharmaceuticals with potential antimicrobial and anti-inflammatory properties. Its structure allows for further functionalization, making it valuable in medicinal chemistry research for designing enzyme inhibitors. Also employed in dye synthesis due to the presence of naphthalene and nitro groups, contributing to chromophoric properties. Serves as a reagent in organic transformations where sulfonamides act as directing groups or protecting moieties.

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