3-Fluoro-4-(trifluoromethoxy)benzoic acid

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Reagent Code: #44812
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CAS Number 886498-89-1

science Other reagents with same CAS 886498-89-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224.1100 g/mol
Formula C₈H₄F₄O₃
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MDL Number MFCD06660202
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Storage room temperature

description Product Description

This chemical is primarily utilized in the synthesis of advanced pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) with specific biological activities. Its unique structure, featuring both fluorine and trifluoromethoxy groups, enhances the metabolic stability and bioavailability of drug molecules. It is often employed in the production of anti-inflammatory, antimicrobial, and anticancer agents, where its electron-withdrawing properties improve binding affinity to target proteins. Additionally, it serves as a key intermediate in organic synthesis for creating fluorinated aromatic compounds, which are valuable in agrochemical research and material science for developing novel pesticides and specialty chemicals.

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Test Parameter Specification
Appearance White to Off-White Solid
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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inventory 1g
10-20 days ฿1,251.00

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3-Fluoro-4-(trifluoromethoxy)benzoic acid
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This chemical is primarily utilized in the synthesis of advanced pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) with specific biological activities. Its unique structure, featuring both fluorine and trifluoromethoxy groups, enhances the metabolic stability and bioavailability of drug molecules. It is often employed in the production of anti-inflammatory, antimicrobial, and anticancer agents, where its electron-withdrawing properties improve binding a

This chemical is primarily utilized in the synthesis of advanced pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) with specific biological activities. Its unique structure, featuring both fluorine and trifluoromethoxy groups, enhances the metabolic stability and bioavailability of drug molecules. It is often employed in the production of anti-inflammatory, antimicrobial, and anticancer agents, where its electron-withdrawing properties improve binding affinity to target proteins. Additionally, it serves as a key intermediate in organic synthesis for creating fluorinated aromatic compounds, which are valuable in agrochemical research and material science for developing novel pesticides and specialty chemicals.

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