4-Acetamidophenylboronic acid

97%

Reagent Code: #90553
label
Alias 4-acetamidophenylboronic acid
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CAS Number 101251-09-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 178.98 g/mol
Formula C₈H₁₀BNO₃
badge Registry Numbers
MDL Number MFCD02179451
thermostat Physical Properties
Melting Point 215-220 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex biaryl compounds in pharmaceutical and material science research. Acts as a boronic acid derivative in the development of sensors for detecting sugars and other diol-containing molecules, leveraging its affinity for cis-diols. Applied in organic synthesis for constructing carbon-carbon bonds, particularly in the preparation of bioactive molecules and drug intermediates. Utilized in the design of covalent organic frameworks (COFs) due to its ability to form stable boronate esters. Plays a role in the development of targeted drug delivery systems, where its boronic acid group facilitates binding to specific biomolecules.

format_list_bulleted Product Specification

Test Parameter Specification
Purity 97-100
Appearance Colorless liquid
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿320.00
inventory 1g
10-20 days ฿1,110.00
inventory 5g
10-20 days ฿4,660.00
inventory 25g
10-20 days ฿18,600.00
4-Acetamidophenylboronic acid
Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex biaryl compounds in pharmaceutical and material science research. Acts as a boronic acid derivative in the development of sensors for detecting sugars and other diol-containing molecules, leveraging its affinity for cis-diols. Applied in organic synthesis for constructing carbon-carbon bonds, particularly in the preparation of bioactive molecules and drug intermediates. Utilized in the design of covalent organic frameworks (COFs) due to its ability to form stable boronate esters. Plays a role in the development of targeted drug delivery systems, where its boronic acid group facilitates binding to specific biomolecules.
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