3-Acetamidophenylboronic acid

98%

Reagent Code: #90121
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Alias 3-acetamidophenylboronic acid
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CAS Number 78887-39-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 178.98 g/mol
Formula C₈H₁₀BNO₃
badge Registry Numbers
MDL Number MFCD00236013
thermostat Physical Properties
Melting Point 135 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

3-Acetamidophenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. It serves as a key intermediate in the synthesis of complex organic molecules due to its boronic acid group, which facilitates the coupling process. Additionally, it is employed in the development of sensors and diagnostic tools, as boronic acids can selectively bind to diols and sugars, enabling applications in glucose monitoring and other biochemical assays. Its role in medicinal chemistry is also notable, as it is used to create compounds with potential therapeutic properties.

format_list_bulleted Product Specification

Test Parameter Specification
Melting point 262-264
Purity (HPLC) 98-100%
Purity (Titration with NaOH) 97.5-102.5
Appearance White to tan powder
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿360.00
inventory 5g
10-20 days ฿1,290.00
inventory 25g
10-20 days ฿5,250.00
3-Acetamidophenylboronic acid
3-Acetamidophenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. It serves as a key intermediate in the synthesis of complex organic molecules due to its boronic acid group, which facilitates the coupling process. Additionally, it is employed in the development of sensors and diagnostic tools, as boronic acids can selectively bind to diols and sugars, enabling applications in glucose monitoring and other biochemical assays. Its role in medicinal chemistry is also notable, as it is used to create compounds with potential therapeutic properties.
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