2-(4-chloro-3-fluorophenyl)-2,2-difluoroacetic acid

93%

Reagent Code: #162268
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CAS Number 1823840-58-9

science Other reagents with same CAS 1823840-58-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224.56 g/mol
Formula C₈H₄ClF₃O₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of selective kinase inhibitors and anti-inflammatory agents. Its unique halogen substitution pattern enhances binding affinity and metabolic stability in drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modulate lipophilicity and electron-withdrawing effects. Also utilized in agrochemical research for designing bioactive molecules with improved environmental stability.

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Test Parameter Specification
Appearance Brown solid
Purity (%) 93-100%
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿10,420.00
inventory 250mg
10-20 days ฿3,970.00

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2-(4-chloro-3-fluorophenyl)-2,2-difluoroacetic acid
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Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of selective kinase inhibitors and anti-inflammatory agents. Its unique halogen substitution pattern enhances binding affinity and metabolic stability in drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modulate lipophilicity and electron-withdrawing effects. Also utilized in agrochemical research for designing bioacti

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of selective kinase inhibitors and anti-inflammatory agents. Its unique halogen substitution pattern enhances binding affinity and metabolic stability in drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modulate lipophilicity and electron-withdrawing effects. Also utilized in agrochemical research for designing bioactive molecules with improved environmental stability.

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