N-Ethyl-p-toluenesulfonamide

98%

Reagent Code: #216966
label
Alias N-ethyl p-toluenesulfonamide; p-toluenesulfonethylamine; 4-toluenesulfonethylamine
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CAS Number 80-39-7

science Other reagents with same CAS 80-39-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.27 g/mol
Formula C₉H₁₃NO₂S
badge Registry Numbers
MDL Number MFCD00048511
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves as a building block in the preparation of sulfonamide-based compounds, which are important in the development of certain drugs, particularly in the design of enzyme inhibitors. Also employed in organic synthesis for nitrogen-containing heterocycles due to its stability and reactivity profile. Its derivatives can be found in some antimicrobial and anti-inflammatory agents. Additionally, it may act as a protecting group for amines in multi-step synthetic routes.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿156.00
inventory 100g
10-20 days ฿390.00
inventory 500g
10-20 days ฿1,230.00
inventory 2.5kg
10-20 days ฿3,162.00

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N-Ethyl-p-toluenesulfonamide
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves as a building block in the preparation of sulfonamide-based compounds, which are important in the development of certain drugs, particularly in the design of enzyme inhibitors. Also employed in organic synthesis for nitrogen-containing heterocycles due to its stability and reactivity profile. Its derivatives can be found in some antimicrobial and anti-inflammatory agents. Additionally, it may act as a protecting grou

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves as a building block in the preparation of sulfonamide-based compounds, which are important in the development of certain drugs, particularly in the design of enzyme inhibitors. Also employed in organic synthesis for nitrogen-containing heterocycles due to its stability and reactivity profile. Its derivatives can be found in some antimicrobial and anti-inflammatory agents. Additionally, it may act as a protecting group for amines in multi-step synthetic routes.

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