(4-Hydroxy-3-(trifluoromethyl)phenyl)boronic acid

97%

Reagent Code: #117587
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CAS Number 1187874-94-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.93 g/mol
Formula C₇H₆BF₃O₃
badge Registry Numbers
MDL Number MFCD18384143
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

(4-Hydroxy-3-(trifluoromethyl)phenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound’s boronic acid group acts as a key intermediate, enabling the creation of complex organic molecules with high precision. Its trifluoromethyl and hydroxyl groups enhance its reactivity and stability, making it suitable for designing biologically active compounds. Additionally, it is employed in the development of sensors and catalysts due to its unique electronic properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿21,456.00
inventory 100mg
10-20 days ฿1,584.00
inventory 250mg
10-20 days ฿2,790.00
inventory 1g
10-20 days ฿7,119.00
(4-Hydroxy-3-(trifluoromethyl)phenyl)boronic acid
(4-Hydroxy-3-(trifluoromethyl)phenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound’s boronic acid group acts as a key intermediate, enabling the creation of complex organic molecules with high precision. Its trifluoromethyl and hydroxyl groups enhance its reactivity and stability, making it suitable for designing biologically active compounds. Additionally, it is employed in the development of sensors and catalysts due to its unique electronic properties.
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