(2,3,5,6-Tetrafluorophenyl)boronic acid

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Reagent Code: #36287
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CAS Number 511295-01-5

science Other reagents with same CAS 511295-01-5

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Weight 193.8914 g/mol
Formula C₆H₃BF₄O₂
badge Registry Numbers
MDL Number MFCD04039310
inventory_2 Storage & Handling
Storage -20°C

description Product Description

(2,3,5,6-Tetrafluorophenyl)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 fluorinated aromatic ring enhances its reactivity and stability, making it suitable for creating complex organic molecules with high precision. Additionally, it is employed in the development of sensors and probes due to its ability to interact with diols and other functional groups, enabling applications in biochemical research and diagnostics. Its unique structure also makes it a useful intermediate in the synthesis of fluorinated compounds, which are often sought after for their enhanced properties in medicinal chemistry.

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inventory 100mg
10-20 days ฿1,746.00

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(2,3,5,6-Tetrafluorophenyl)boronic acid
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(2,3,5,6-Tetrafluorophenyl)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 fluorinated aromatic ring enhances its reactivity and stability, making it suitable for creating complex organic molecules with high precision. Additionally, it is employed in the development of sensors a

(2,3,5,6-Tetrafluorophenyl)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 fluorinated aromatic ring enhances its reactivity and stability, making it suitable for creating complex organic molecules with high precision. Additionally, it is employed in the development of sensors and probes due to its ability to interact with diols and other functional groups, enabling applications in biochemical research and diagnostics. Its unique structure also makes it a useful intermediate in the synthesis of fluorinated compounds, which are often sought after for their enhanced properties in medicinal chemistry.

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