2-[3-(4-METHYLBENZOYL)PHENYL]PROPIONIC ACID

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Reagent Code: #214450
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CAS Number 107257-20-5

science Other reagents with same CAS 107257-20-5

blur_circular Chemical Specifications

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Weight 268.31 g/mol
Formula C₁₇H₁₆O₃
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MDL Number MFCD27966872
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as an intermediate in the synthesis of nonsteroidal anti-inflammatory drugs (NSAIDs), particularly in the production of benzophenone-based derivatives with analgesic and antipyretic properties. Its structure supports activity as a cyclooxygenase (COX) inhibitor, contributing to reduced prostaglandin synthesis. Commonly employed in pharmaceutical research for developing anti-inflammatory agents with improved selectivity and reduced side effects. Also utilized in the preparation of photostable organic compounds due to the benzophenone moiety, making it valuable in UV-absorbing materials and dermatological formulations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿26,630.00
inventory 250mg
10-20 days ฿45,250.00

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2-[3-(4-METHYLBENZOYL)PHENYL]PROPIONIC ACID
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Used primarily as an intermediate in the synthesis of nonsteroidal anti-inflammatory drugs (NSAIDs), particularly in the production of benzophenone-based derivatives with analgesic and antipyretic properties. Its structure supports activity as a cyclooxygenase (COX) inhibitor, contributing to reduced prostaglandin synthesis. Commonly employed in pharmaceutical research for developing anti-inflammatory agents with improved selectivity and reduced side effects. Also utilized in the preparation of photostab

Used primarily as an intermediate in the synthesis of nonsteroidal anti-inflammatory drugs (NSAIDs), particularly in the production of benzophenone-based derivatives with analgesic and antipyretic properties. Its structure supports activity as a cyclooxygenase (COX) inhibitor, contributing to reduced prostaglandin synthesis. Commonly employed in pharmaceutical research for developing anti-inflammatory agents with improved selectivity and reduced side effects. Also utilized in the preparation of photostable organic compounds due to the benzophenone moiety, making it valuable in UV-absorbing materials and dermatological formulations.

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