2-(4-bromo-3-methoxyphenyl)-2,2-difluoroacetic acid

96%

Reagent Code: #148904
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CAS Number 2228694-85-5

science Other reagents with same CAS 2228694-85-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 281.05 g/mol
Formula C₉H₇BrF₂O₃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and anti-inflammatory agents. Its structure allows for selective modification in drug design, enhancing potency and metabolic stability. Commonly employed in research settings for creating analogs in medicinal chemistry programs targeting cancer and autoimmune diseases. The bromo and methoxy functional groups enable cross-coupling reactions, facilitating rapid diversification during lead optimization. Also utilized in agrochemical research for developing bioactive molecules with improved environmental stability.

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Test Parameter Specification
Appearance White solid
Purity (%) 96-100%
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,980.00
inventory 250mg
10-20 days ฿3,600.00
inventory 1g
10-20 days ฿9,360.00

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2-(4-bromo-3-methoxyphenyl)-2,2-difluoroacetic acid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and anti-inflammatory agents. Its structure allows for selective modification in drug design, enhancing potency and metabolic stability. Commonly employed in research settings for creating analogs in medicinal chemistry programs targeting cancer and autoimmune diseases. The bromo and methoxy functional groups enable cross-coupling reactions, facilitating rapid diversification duri

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and anti-inflammatory agents. Its structure allows for selective modification in drug design, enhancing potency and metabolic stability. Commonly employed in research settings for creating analogs in medicinal chemistry programs targeting cancer and autoimmune diseases. The bromo and methoxy functional groups enable cross-coupling reactions, facilitating rapid diversification during lead optimization. Also utilized in agrochemical research for developing bioactive molecules with improved environmental stability.

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