2-Oxo-2-(4-phenylphenyl)acetic acid

95%

Reagent Code: #130319
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CAS Number 5449-21-8

science Other reagents with same CAS 5449-21-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.23 g/mol
Formula C₁₄H₁₀O₃
badge Registry Numbers
MDL Number MFCD11179638
thermostat Physical Properties
Melting Point 101-103 °C
Boiling Point 397.8±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.250±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly in the production of biphenyl-based pharmaceuticals. Its structure allows for efficient coupling reactions in organic synthesis, making it valuable in developing analgesic and antipyretic agents. Also employed in the preparation of photoinitiators for polymer chemistry due to its ability to generate radicals under UV light. Its aromatic ketone functionality supports use in material science for designing functional organic compounds.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,300.00

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2-Oxo-2-(4-phenylphenyl)acetic 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 biphenyl-based pharmaceuticals. Its structure allows for efficient coupling reactions in organic synthesis, making it valuable in developing analgesic and antipyretic agents. Also employed in the preparation of photoinitiators for polymer chemistry due to its ability to generate radicals under UV light. Its aromatic ketone functionality supports use in material science for desi

Used as a key intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly in the production of biphenyl-based pharmaceuticals. Its structure allows for efficient coupling reactions in organic synthesis, making it valuable in developing analgesic and antipyretic agents. Also employed in the preparation of photoinitiators for polymer chemistry due to its ability to generate radicals under UV light. Its aromatic ketone functionality supports use in material science for designing functional organic compounds.

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