N-(2,6-Dichlorophenyl)-2-phenylacetamide

98%

Reagent Code: #220293
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CAS Number 304884-75-1

science Other reagents with same CAS 304884-75-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 280.15 g/mol
Formula C₁₄H₁₁Cl₂NO
badge Registry Numbers
MDL Number MFCD00578391
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs). It serves as a key building block in the preparation of phenylalkanoic acid derivatives, which exhibit analgesic and antipyretic properties. Its structure allows for selective chemical modifications, making it valuable in medicinal chemistry for developing compounds with improved bioavailability and reduced side effects. Also employed in research settings for exploring new drug candidates targeting inflammation and pain pathways.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,050.00
inventory 250mg
10-20 days ฿20,460.00
inventory 1g
10-20 days ฿67,800.00
N-(2,6-Dichlorophenyl)-2-phenylacetamide
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Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs). It serves as a key building block in the preparation of phenylalkanoic acid derivatives, which exhibit analgesic and antipyretic properties. Its structure allows for selective chemical modifications, making it valuable in medicinal chemistry for developing compounds with improved bioavailability and reduced side effects. Also employed in research setting

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs). It serves as a key building block in the preparation of phenylalkanoic acid derivatives, which exhibit analgesic and antipyretic properties. Its structure allows for selective chemical modifications, making it valuable in medicinal chemistry for developing compounds with improved bioavailability and reduced side effects. Also employed in research settings for exploring new drug candidates targeting inflammation and pain pathways.

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