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

93%

Reagent Code: #162260
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CAS Number 1027514-19-7

science Other reagents with same CAS 1027514-19-7

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. Its unique halogen substitution pattern enhances binding affinity and metabolic stability in drug candidates. Commonly employed in oncology research for constructing active pharmaceutical ingredients requiring high lipophilicity and electron-withdrawing properties. Also utilized in agrochemicals for creating herbicides with improved environmental persistence and target specificity.

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Test Parameter Specification
Appearance White Solid
Purity (%) 92.5-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,651.00
inventory 250mg
10-20 days ฿4,284.50
inventory 1g
10-20 days ฿11,137.50

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2-(3-chloro-4-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. Its unique halogen substitution pattern enhances binding affinity and metabolic stability in drug candidates. Commonly employed in oncology research for constructing active pharmaceutical ingredients requiring high lipophilicity and electron-withdrawing properties. Also utilized in agrochemicals for creating herbicides with improved environmental persistence and targ

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of selective kinase inhibitors. Its unique halogen substitution pattern enhances binding affinity and metabolic stability in drug candidates. Commonly employed in oncology research for constructing active pharmaceutical ingredients requiring high lipophilicity and electron-withdrawing properties. Also utilized in agrochemicals for creating herbicides with improved environmental persistence and target specificity.

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