N-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acrylamide

98%

Reagent Code: #91018
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CAS Number 874363-18-5

science Other reagents with same CAS 874363-18-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 273.14 g/mol
Formula C₁₅H₂₀BNO₃
badge Registry Numbers
MDL Number MFCD22493996
thermostat Physical Properties
Melting Point 160℃
inventory_2 Storage & Handling
Storage 2-8℃, dry

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in the field of polymer chemistry and materials science. It serves as a key monomer in the production of advanced polymeric materials, enabling the incorporation of boronate ester functionalities into polymer chains. These functionalities are valuable for creating stimuli-responsive materials, such as those that react to changes in pH, glucose levels, or other biological conditions, making it useful in biomedical applications like drug delivery systems and biosensors. Additionally, its acrylamide group allows for polymerization via radical mechanisms, facilitating the development of hydrogels and other cross-linked networks. The compound is also employed in the synthesis of organic electronic materials, where its boronate ester group can participate in cross-coupling reactions, contributing to the fabrication of conjugated polymers for optoelectronic devices.

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Test Parameter Specification
Appearance White to off-white solid
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,430.00

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N-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acrylamide
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This chemical is primarily utilized in organic synthesis, particularly in the field of polymer chemistry and materials science. It serves as a key monomer in the production of advanced polymeric materials, enabling the incorporation of boronate ester functionalities into polymer chains. These functionalities are valuable for creating stimuli-responsive materials, such as those that react to changes in pH, glucose levels, or other biological conditions, making it useful in biomedical applications like dru

This chemical is primarily utilized in organic synthesis, particularly in the field of polymer chemistry and materials science. It serves as a key monomer in the production of advanced polymeric materials, enabling the incorporation of boronate ester functionalities into polymer chains. These functionalities are valuable for creating stimuli-responsive materials, such as those that react to changes in pH, glucose levels, or other biological conditions, making it useful in biomedical applications like drug delivery systems and biosensors. Additionally, its acrylamide group allows for polymerization via radical mechanisms, facilitating the development of hydrogels and other cross-linked networks. The compound is also employed in the synthesis of organic electronic materials, where its boronate ester group can participate in cross-coupling reactions, contributing to the fabrication of conjugated polymers for optoelectronic devices.

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