3-(6-Trifluoromethylpyridin-2-yl)phenylboronic acid

95%

Reagent Code: #91829
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CAS Number 2225180-52-7

science Other reagents with same CAS 2225180-52-7

blur_circular Chemical Specifications

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Weight 267.0115696 g/mol
Formula C₁₂H₉BF₃NO₂
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

This compound is widely utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. It is often employed in the synthesis of complex molecules, including bioactive compounds and polymers, due to its stability and reactivity. Additionally, it serves as a key intermediate in the development of drug candidates, especially in medicinal chemistry research targeting various diseases. Its trifluoromethyl group enhances its lipophilicity, which can improve the pharmacokinetic properties of the resulting compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿120,600.00
inventory 5mg
10-20 days ฿13,400.00
inventory 25mg
10-20 days ฿40,200.00

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3-(6-Trifluoromethylpyridin-2-yl)phenylboronic acid
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This compound is widely utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. It is often employed in the synthesis of complex molecules, including bioactive compounds and polymers, due to its stability and reactivity. Additionally, it serves as a key intermediate in the development of dr

This compound is widely utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. It is often employed in the synthesis of complex molecules, including bioactive compounds and polymers, due to its stability and reactivity. Additionally, it serves as a key intermediate in the development of drug candidates, especially in medicinal chemistry research targeting various diseases. Its trifluoromethyl group enhances its lipophilicity, which can improve the pharmacokinetic properties of the resulting compounds.

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