4-Hydroxyphenylboronic acid

97%

Reagent Code: #90715
label
Alias 4-Hydroxyphenylboronic acid; 4-Hydroxyphenylboronic acid
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CAS Number 71597-85-8

science Other reagents with same CAS 71597-85-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 137.93 g/mol
Formula C₆H₇BO₃
badge Registry Numbers
MDL Number MFCD01074628
thermostat Physical Properties
Melting Point >230 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

4-Hydroxyphenylboronic acid is widely used in organic synthesis as a key building block for creating complex molecules. It plays a significant role in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds in pharmaceuticals and advanced materials. In medicinal chemistry, it is utilized to develop bioactive compounds and drug candidates, particularly in targeting enzymes or receptors. Additionally, it serves as a sensor component in glucose detection systems due to its ability to bind diols, making it valuable in diabetes management tools. Its applications also extend to polymer chemistry, where it is used to design functional materials with specific properties.

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Test Parameter Specification
Melting point 230-260
Purity (LC) 96.5-100%
Appearance White to off-white to orange to red to brown powder or crystals
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿340.00
inventory 5g
10-20 days ฿780.00
inventory 25g
10-20 days ฿2,430.00
inventory 100g
10-20 days ฿9,080.00

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4-Hydroxyphenylboronic acid
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4-Hydroxyphenylboronic acid is widely used in organic synthesis as a key building block for creating complex molecules. It plays a significant role in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds in pharmaceuticals and advanced materials. In medicinal chemistry, it is utilized to develop bioactive compounds and drug candidates, particularly in targeting enzymes or receptors. Additionally, it serves as a sensor component in glucose detection systems due to its ability to bind diols, making it valuable in diabetes management tools. Its applications also extend to polymer chemistry, where it is used to design functional materials with specific properties.
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