2-(3-cyanophenyl)-2-methylpropanoic acid

95%

Reagent Code: #162237
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CAS Number 445003-63-4

science Other reagents with same CAS 445003-63-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.08 g/mol
Formula C₁₁H₁₁NO₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a key intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly in the production of fenoprofen and related analogs. Its structure allows for efficient derivatization to form active pharmaceutical ingredients with analgesic and antipyretic properties. Commonly employed in research and development of new anti-inflammatory compounds due to its reactive functional groups, which facilitate coupling reactions and molecular modifications. Also utilized in the preparation of chiral building blocks for asymmetric synthesis in medicinal chemistry.

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Test Parameter Specification
Appearance White liquid
Purity (%) 95-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,250.00

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2-(3-cyanophenyl)-2-methylpropanoic acid
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Used as a key intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly in the production of fenoprofen and related analogs. Its structure allows for efficient derivatization to form active pharmaceutical ingredients with analgesic and antipyretic properties. Commonly employed in research and development of new anti-inflammatory compounds due to its reactive functional groups, which facilitate coupling reactions and molecular modifications. Also utilized in the prepara

Used as a key intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly in the production of fenoprofen and related analogs. Its structure allows for efficient derivatization to form active pharmaceutical ingredients with analgesic and antipyretic properties. Commonly employed in research and development of new anti-inflammatory compounds due to its reactive functional groups, which facilitate coupling reactions and molecular modifications. Also utilized in the preparation of chiral building blocks for asymmetric synthesis in medicinal chemistry.

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