(6-Ethoxy-5-(trifluoromethyl)pyridin-3-yl)boronic acid

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Reagent Code: #183878
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CAS Number 849934-85-6

science Other reagents with same CAS 849934-85-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.97 g/mol
Formula C₈H₉BF₃NO₃
badge Registry Numbers
MDL Number MFCD13195241
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for targeted cancer therapies. Its boronic acid functional group enables Suzuki-Miyaura cross-coupling reactions, allowing efficient construction of biaryl structures commonly found in bioactive molecules. It is also employed in medicinal chemistry research to modify pyridine-based scaffolds, enhancing metabolic stability and binding affinity. The presence of trifluoromethyl and ethoxy groups contributes to improved lipophilicity and pharmacokinetic properties in drug candidates.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿28,480.00
inventory 1g
10-20 days ฿51,200.00
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(6-Ethoxy-5-(trifluoromethyl)pyridin-3-yl)boronic acid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for targeted cancer therapies. Its boronic acid functional group enables Suzuki-Miyaura cross-coupling reactions, allowing efficient construction of biaryl structures commonly found in bioactive molecules. It is also employed in medicinal chemistry research to modify pyridine-based scaffolds, enhancing metabolic stability and binding affinity. The presence of trifluoromethyl and e

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for targeted cancer therapies. Its boronic acid functional group enables Suzuki-Miyaura cross-coupling reactions, allowing efficient construction of biaryl structures commonly found in bioactive molecules. It is also employed in medicinal chemistry research to modify pyridine-based scaffolds, enhancing metabolic stability and binding affinity. The presence of trifluoromethyl and ethoxy groups contributes to improved lipophilicity and pharmacokinetic properties in drug candidates.

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