2-Ethyl-6-(trifluoromethyl)pyridine-4-boronic acid

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Reagent Code: #59426
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CAS Number 2225170-32-9

science Other reagents with same CAS 2225170-32-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.9687696 g/mol
Formula C₈H₉BF₃NO₂
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for the introduction of the pyridine moiety into more complex molecules, which is valuable in the development of pharmaceuticals and agrochemicals. Its trifluoromethyl group enhances the lipophilicity and metabolic stability of the resulting compounds, making it useful in drug discovery. Additionally, it finds applications in material science, where it contributes to the synthesis of advanced organic materials with specific electronic properties.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿29,700.00
inventory 5mg
10-20 days ฿8,982.00
inventory 100mg
10-20 days ฿82,800.00
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2-Ethyl-6-(trifluoromethyl)pyridine-4-boronic acid
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for the introduction of the pyridine moiety into more complex molecules, which is valuable in the development of pharmaceuticals and agrochemicals. Its trifluoromethyl group enhances the lipophilicity and metabolic stability of the resulting compounds, making it useful in drug discovery. Additionally, it finds applications in material sc

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for the introduction of the pyridine moiety into more complex molecules, which is valuable in the development of pharmaceuticals and agrochemicals. Its trifluoromethyl group enhances the lipophilicity and metabolic stability of the resulting compounds, making it useful in drug discovery. Additionally, it finds applications in material science, where it contributes to the synthesis of advanced organic materials with specific electronic properties.

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