3-Trifluoromethyl-5-(piperidin-4-yl)phenylboronic acid

95%

Reagent Code: #91973
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CAS Number 2225170-15-8

science Other reagents with same CAS 2225170-15-8

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Weight 273.0592096 g/mol
Formula C₁₂H₁₅BF₃NO₂
inventory_2 Storage & Handling
Storage -20℃

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research. The boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl structures, which are common in drug candidates. The trifluoromethyl group enhances the compound's stability and can influence the pharmacokinetic properties of the resulting molecules. The piperidin-4-yl substituent provides opportunities for further derivatization and improves interactions with biological targets, contributing to specificity in bioactive compounds. Its application extends to the development of new materials and agrochemicals, where its unique structure contributes to the desired chemical and physical properties.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿52,920.00

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3-Trifluoromethyl-5-(piperidin-4-yl)phenylboronic acid
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research. The boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl structures, which are common in drug candidates. The trifluoromethyl group enhances the compound's stability and can influence the pharmacokinetic properties of the resulting molecu

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research. The boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl structures, which are common in drug candidates. The trifluoromethyl group enhances the compound's stability and can influence the pharmacokinetic properties of the resulting molecules. The piperidin-4-yl substituent provides opportunities for further derivatization and improves interactions with biological targets, contributing to specificity in bioactive compounds. Its application extends to the development of new materials and agrochemicals, where its unique structure contributes to the desired chemical and physical properties.

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