3-Aminophenylboronic acid monohydrate

97%

Reagent Code: #90189
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Alias 3-Aminophenylboronic acid monohydrate; 3-aminophenylboronic acid hydrate; 3-aminophenylboronic acid (monohydrate); 3-aminophenylboronic acid monohydrate; m-aminophenylboronic acid monohydrate; m-aminophenylboronic acid hydrate ; m-aminophenylboronic acid monohydrate; m-aminophenylboronic acid (monohydrate)
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CAS Number 206658-89-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 154.96 g/mol
Formula C₆H₈BNO₂H₂O
badge Registry Numbers
MDL Number MFCD00149554
thermostat Physical Properties
Melting Point 94 °C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

This compound is widely utilized in organic synthesis, particularly as a key reagent in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in creating complex organic molecules. Additionally, it serves as a building block in the development of sensors and diagnostic tools due to its ability to interact with diols and sugars, making it useful in glucose sensing applications. It is also employed in the preparation of boron-containing polymers and materials for various industrial applications.

format_list_bulleted Product Specification

Test Parameter Specification
Melting Point 93-96
Purity (HPLC) 97-100
Purity (Neutralization Titration) 97.5-102.5
Appearance White to tan powder or crystals
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days $24.27
inventory 5g
10-20 days $81.26
inventory 25g
10-20 days $285.45
inventory 100g
10-20 days $980.88
3-Aminophenylboronic acid monohydrate
This compound is widely utilized in organic synthesis, particularly as a key reagent in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in creating complex organic molecules. Additionally, it serves as a building block in the development of sensors and diagnostic tools due to its ability to interact with diols and sugars, making it useful in glucose sensing applications. It is also employed in the preparation of boron-containing polymers and materials for various industrial applications.
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