4-Vinylphenylboronic acid

96%

Reagent Code: #90551
label
Alias 4-vinylphenylboronic acid
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CAS Number 2156-04-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 147.97 g/mol
Formula C₈H₉BO₂
badge Registry Numbers
MDL Number MFCD00239441
thermostat Physical Properties
Melting Point 190-193°C
inventory_2 Storage & Handling
Density 1.09g/mL
Storage 2~8°C

description Product Description

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, it facilitates the synthesis of biaryl compounds, which are essential in pharmaceuticals and organic electronics. It is also employed in the preparation of functional polymers and materials, particularly those requiring boronic acid groups for sensing or molecular recognition applications. Its vinyl group allows for polymerization, making it useful in creating advanced materials like hydrogels or coatings with specific binding properties. Additionally, it plays a role in developing biosensors and drug delivery systems due to its ability to interact with diols and sugars.

format_list_bulleted Product Specification

Test Parameter Specification
Purity 95.5-100%
Melting point 190-193
Appearance White to light brown powder or crystals
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿10,600.00
inventory 1g
10-20 days ฿630.00
inventory 5g
10-20 days ฿2,590.00
inventory 100g
10-20 days ฿40,260.00
4-Vinylphenylboronic acid
Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, it facilitates the synthesis of biaryl compounds, which are essential in pharmaceuticals and organic electronics. It is also employed in the preparation of functional polymers and materials, particularly those requiring boronic acid groups for sensing or molecular recognition applications. Its vinyl group allows for polymerization, making it useful in creating advanced materials like hydrogels or coatings with specific binding properties. Additionally, it plays a role in developing biosensors and drug delivery systems due to its ability to interact with diols and sugars.
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