4-(Hydroxymethyl)phenylboronic acid

≥99%

Reagent Code: #90718
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Alias 4-Hydroxymethylphenylboronic acid
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CAS Number 59016-93-2

science Other reagents with same CAS 59016-93-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 151.96 g/mol
Formula C₇H₉BO₃
badge Registry Numbers
MDL Number MFCD00792672
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used in organic synthesis as a key reagent for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Commonly employed in the preparation of biaryl compounds, which are important in pharmaceuticals and materials science. Acts as a boronic acid derivative in the development of sensors for detecting sugars and other diols due to its ability to form stable cyclic esters. Applied in the production of advanced polymers and coatings, enhancing their functional properties. Also utilized in medicinal chemistry for the design of enzyme inhibitors and drug candidates, particularly in targeting diseases like cancer and diabetes.

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Test Parameter Specification
Appearance Solid
Purity 98.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿660.00
inventory 5g
10-20 days ฿1,580.00
inventory 25g
10-20 days ฿4,470.00

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4-(Hydroxymethyl)phenylboronic acid
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Used in organic synthesis as a key reagent for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Commonly employed in the preparation of biaryl compounds, which are important in pharmaceuticals and materials science. Acts as a boronic acid derivative in the development of sensors for detecting sugars and other diols due to its ability to form stable cyclic esters. Applied in the production of advanced polymers and coatings, enhancing their functional properties. Also

Used in organic synthesis as a key reagent for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Commonly employed in the preparation of biaryl compounds, which are important in pharmaceuticals and materials science. Acts as a boronic acid derivative in the development of sensors for detecting sugars and other diols due to its ability to form stable cyclic esters. Applied in the production of advanced polymers and coatings, enhancing their functional properties. Also utilized in medicinal chemistry for the design of enzyme inhibitors and drug candidates, particularly in targeting diseases like cancer and diabetes.

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