N-(5-Cyano-2-methylphenyl)acetamide

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Reagent Code: #215904
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CAS Number 81018-31-7

science Other reagents with same CAS 81018-31-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.2 g/mol
Formula C₁₀H₁₀N₂O
badge Registry Numbers
MDL Number MFCD16683000
thermostat Physical Properties
Melting Point 153-154 °C(Solv: ethanol (64-17-5))
Boiling Point 360.1±30.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.13±0.1 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its structure supports the construction of more complex aromatic amide derivatives with potential analgesic and antipyretic properties. Also employed in agrochemical research for designing herbicides and plant growth regulators due to its stability and reactivity in coupling reactions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿890.00
inventory 1g
10-20 days ฿2,400.00
inventory 5g
10-20 days ฿9,100.00

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N-(5-Cyano-2-methylphenyl)acetamide
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its structure supports the construction of more complex aromatic amide derivatives with potential analgesic and antipyretic properties. Also employed in agrochemical research for designing herbicides and plant growth regulators due to its stability and reactivity in coupling reactions.

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its structure supports the construction of more complex aromatic amide derivatives with potential analgesic and antipyretic properties. Also employed in agrochemical research for designing herbicides and plant growth regulators due to its stability and reactivity in coupling reactions.

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