2-Acrylamidophenylboronic acid pinacol ester

95%

Reagent Code: #42251
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CAS Number 1218790-42-1

science Other reagents with same CAS 1218790-42-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 291 g/mol
Formula C₁₅H₂₀BNO₃
badge Registry Numbers
MDL Number MFCD10700144
inventory_2 Storage & Handling
Storage 2-8℃, dry, airtight

description Product Description

This compound is primarily utilized in the field of polymer chemistry and materials science. It serves as a functional monomer in the synthesis of stimuli-responsive polymers, particularly those designed to interact with diol-containing molecules, such as glucose. Its boronic acid ester group enables it to form reversible covalent bonds with diols, making it valuable in the development of glucose-sensitive hydrogels for biomedical applications, including glucose sensors and drug delivery systems. Additionally, it is employed in the creation of advanced materials for molecular recognition and separation processes, where selective binding to specific analytes is required. Its unique properties also make it suitable for use in surface modification and functionalization of nanoparticles for targeted applications.

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Test Parameter Specification
Appearance white solid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,998.00
inventory 250mg
10-20 days ฿3,339.00
inventory 1g
10-20 days ฿8,883.00

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2-Acrylamidophenylboronic acid pinacol ester
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This compound is primarily utilized in the field of polymer chemistry and materials science. It serves as a functional monomer in the synthesis of stimuli-responsive polymers, particularly those designed to interact with diol-containing molecules, such as glucose. Its boronic acid ester group enables it to form reversible covalent bonds with diols, making it valuable in the development of glucose-sensitive hydrogels for biomedical applications, including glucose sensors and drug delivery systems. Additio

This compound is primarily utilized in the field of polymer chemistry and materials science. It serves as a functional monomer in the synthesis of stimuli-responsive polymers, particularly those designed to interact with diol-containing molecules, such as glucose. Its boronic acid ester group enables it to form reversible covalent bonds with diols, making it valuable in the development of glucose-sensitive hydrogels for biomedical applications, including glucose sensors and drug delivery systems. Additionally, it is employed in the creation of advanced materials for molecular recognition and separation processes, where selective binding to specific analytes is required. Its unique properties also make it suitable for use in surface modification and functionalization of nanoparticles for targeted applications.

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