(2S)-2-(4-Fluorophenyl)-2-hydroxyacetic acid

95%

Reagent Code: #236985
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CAS Number 52923-25-8

science Other reagents with same CAS 52923-25-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 170.1378 g/mol
Formula C₈H₇FO₃
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of fluorinated analogs of bioactive molecules. Its hydroxy acid functionality and stereochemistry make it valuable for constructing complex drug scaffolds, especially in antifungal and anti-inflammatory agents. The fluorophenyl group enhances metabolic stability and membrane permeability, making derivatives useful in medicinal chemistry. Also employed in asymmetric synthesis to introduce fluorinated motifs with high enantioselectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,280.00
inventory 250mg
10-20 days ฿3,700.00
inventory 1g
10-20 days ฿10,400.00
inventory 5g
10-20 days ฿42,490.00
(2S)-2-(4-Fluorophenyl)-2-hydroxyacetic acid
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of fluorinated analogs of bioactive molecules. Its hydroxy acid functionality and stereochemistry make it valuable for constructing complex drug scaffolds, especially in antifungal and anti-inflammatory agents. The fluorophenyl group enhances metabolic stability and membrane permeability, making derivatives useful in medicinal chemistry. Also employed in asymmetric synthesis to introduce fluorinated motifs w

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of fluorinated analogs of bioactive molecules. Its hydroxy acid functionality and stereochemistry make it valuable for constructing complex drug scaffolds, especially in antifungal and anti-inflammatory agents. The fluorophenyl group enhances metabolic stability and membrane permeability, making derivatives useful in medicinal chemistry. Also employed in asymmetric synthesis to introduce fluorinated motifs with high enantioselectivity.

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