N-(2-Ethoxy-4-nitrophenyl)acetamide

95%

Reagent Code: #218807
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CAS Number 116496-76-5

science Other reagents with same CAS 116496-76-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224.21 g/mol
Formula C₁₀H₁₂N₂O₄
badge Registry Numbers
MDL Number MFCD00994990
thermostat Physical Properties
Boiling Point 416.2 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used as an intermediate in the synthesis of azo dyes and pigments, particularly for producing yellow and orange shades in textile and printing inks. It is valued for its role in coupling reactions due to the presence of the nitro and ethoxy groups, which influence solubility and reactivity. Also employed in the preparation of certain pharmaceuticals and agrochemicals where nitroaromatic derivatives are required. Its acetamide functionality allows for further chemical modifications, making it useful in organic synthesis and research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿980.00
inventory 5g
10-20 days ฿4,570.00
inventory 25g
10-20 days ฿20,030.00
N-(2-Ethoxy-4-nitrophenyl)acetamide
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Used as an intermediate in the synthesis of azo dyes and pigments, particularly for producing yellow and orange shades in textile and printing inks. It is valued for its role in coupling reactions due to the presence of the nitro and ethoxy groups, which influence solubility and reactivity. Also employed in the preparation of certain pharmaceuticals and agrochemicals where nitroaromatic derivatives are required. Its acetamide functionality allows for further chemical modifications, making it useful in organ
Used as an intermediate in the synthesis of azo dyes and pigments, particularly for producing yellow and orange shades in textile and printing inks. It is valued for its role in coupling reactions due to the presence of the nitro and ethoxy groups, which influence solubility and reactivity. Also employed in the preparation of certain pharmaceuticals and agrochemicals where nitroaromatic derivatives are required. Its acetamide functionality allows for further chemical modifications, making it useful in organic synthesis and research.
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