N-(3-(Diethylamino)-4-methoxyphenyl)acetamide

98%

Reagent Code: #219669
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CAS Number 19433-93-3

science Other reagents with same CAS 19433-93-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.31 g/mol
Formula C₁₃H₂₀N₂O₂
badge Registry Numbers
MDL Number MFCD01075759
thermostat Physical Properties
Melting Point 93-97 °C(lit.)
Boiling Point 389.5±32.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.086±0.06 g/cm3(Predicted)
Storage Room temperature, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of analgesic and anti-inflammatory agents. Its structure supports activity in central nervous system-targeted drugs due to the presence of amide and methoxy functionalities. Commonly employed in research settings for designing novel compounds with potential pain-relieving effects. Also utilized in the preparation of dyes and functional materials where electron-donating groups enhance optical properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿800.00
inventory 25g
10-20 days ฿2,680.00
N-(3-(Diethylamino)-4-methoxyphenyl)acetamide
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of analgesic and anti-inflammatory agents. Its structure supports activity in central nervous system-targeted drugs due to the presence of amide and methoxy functionalities. Commonly employed in research settings for designing novel compounds with potential pain-relieving effects. Also utilized in the preparation of dyes and functional materials where electron-donating groups enhance optical properties.

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of analgesic and anti-inflammatory agents. Its structure supports activity in central nervous system-targeted drugs due to the presence of amide and methoxy functionalities. Commonly employed in research settings for designing novel compounds with potential pain-relieving effects. Also utilized in the preparation of dyes and functional materials where electron-donating groups enhance optical properties.

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