2-(2,6-Difluorophenyl)-2-methylpropanoic acid

98%

Reagent Code: #177848
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CAS Number 1216838-87-7

science Other reagents with same CAS 1216838-87-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.185 g/mol
Formula C₁₀H₁₀F₂O₂
badge Registry Numbers
MDL Number MFCD11036902
thermostat Physical Properties
Boiling Point 284.1±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.257±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly in the production of flurbiprofen analogs. Its fluorinated aromatic structure enhances metabolic stability and bioavailability in pharmaceutical applications. Commonly employed in research settings to develop chiral compounds with improved analgesic and anti-inflammatory properties. Also utilized in the preparation of prodrugs and derivatives aimed at reducing gastrointestinal side effects associated with traditional NSAIDs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿380.00
inventory 250mg
10-20 days ฿920.00
inventory 1g
10-20 days ฿3,520.00

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2-(2,6-Difluorophenyl)-2-methylpropanoic acid
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Used as an intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly in the production of flurbiprofen analogs. Its fluorinated aromatic structure enhances metabolic stability and bioavailability in pharmaceutical applications. Commonly employed in research settings to develop chiral compounds with improved analgesic and anti-inflammatory properties. Also utilized in the preparation of prodrugs and derivatives aimed at reducing gastrointestinal side effects associated

Used as an intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly in the production of flurbiprofen analogs. Its fluorinated aromatic structure enhances metabolic stability and bioavailability in pharmaceutical applications. Commonly employed in research settings to develop chiral compounds with improved analgesic and anti-inflammatory properties. Also utilized in the preparation of prodrugs and derivatives aimed at reducing gastrointestinal side effects associated with traditional NSAIDs.

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