3-Fluorophenylboronic acid

97%

Reagent Code: #90183
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Alias 3-fluorophenylboronic acid; 3-fluorophenylboronic acid, m-fluorophenylboronic acid
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CAS Number 768-35-4

science Other reagents with same CAS 768-35-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 139.92 g/mol
Formula C₆H₆BFO₂
badge Registry Numbers
MDL Number MFCD00236042
thermostat Physical Properties
Melting Point 214-218 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

3-Fluorophenylboronic 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 serves as a key intermediate in the synthesis of various biologically active molecules, including drug candidates targeting cancer, inflammation, and infectious diseases. Additionally, it is employed in the development of sensors and diagnostic tools due to its ability to interact with diols and other functional groups, making it useful in glucose sensing and other analytical applications. Its versatility and reactivity make it a crucial component in modern chemical research and industrial processes.

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Test Parameter Specification
Purity 97-100%
Appearance White to off-white powder or crystals
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿320.00
inventory 5g
10-20 days ฿570.00
inventory 25g
10-20 days ฿1,160.00
inventory 100g
10-20 days ฿3,920.00
inventory 500g
10-20 days ฿19,470.00

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3-Fluorophenylboronic acid
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3-Fluorophenylboronic 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 serves as a key intermediate in the synthesis of various biologically active molecules, including drug candidates targeting cancer, inflammation, and infectious diseases. Additionally, it is employed in the development

3-Fluorophenylboronic 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 serves as a key intermediate in the synthesis of various biologically active molecules, including drug candidates targeting cancer, inflammation, and infectious diseases. Additionally, it is employed in the development of sensors and diagnostic tools due to its ability to interact with diols and other functional groups, making it useful in glucose sensing and other analytical applications. Its versatility and reactivity make it a crucial component in modern chemical research and industrial processes.

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