2-Trifluoromethyl-6-(piperidin-3-yl)pyridine-4-boronic acid

95%

Reagent Code: #91788
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CAS Number 2225153-03-5

science Other reagents with same CAS 2225153-03-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 274.0472696 g/mol
Formula C₁₁H₁₄BF₃N₂O₂
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. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable for constructing complex molecules in pharmaceutical and agrochemical research. Additionally, its trifluoromethyl and piperidinyl groups contribute to its potential as a building block for designing bioactive compounds, including drug candidates targeting neurological or metabolic disorders. The compound’s unique structure also makes it suitable for use in material science, particularly in the development of advanced organic materials with specific electronic or optical properties.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿223,800.00
inventory 5mg
10-20 days ฿86,080.00

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2-Trifluoromethyl-6-(piperidin-3-yl)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. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable for constructing complex molecules in pharmaceutical and agrochemical research. Additionally, its trifluoromethyl and piperidinyl groups contribute to its potential as a building block for designing bioactive compounds, including drug candidates targeting neurological or metabolic dis

This compound is primarily 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 for constructing complex molecules in pharmaceutical and agrochemical research. Additionally, its trifluoromethyl and piperidinyl groups contribute to its potential as a building block for designing bioactive compounds, including drug candidates targeting neurological or metabolic disorders. The compound’s unique structure also makes it suitable for use in material science, particularly in the development of advanced organic materials with specific electronic or optical properties.

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