3-Aminophenylboronic acid monohydrate
97%
Reagent
Code: #90189
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)
CAS Number
206658-89-1
blur_circular Chemical Specifications
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Molecular Information
Weight
154.96 g/mol
Formula
C₆H₈BNO₂H₂O
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Registry Numbers
MDL Number
MFCD00149554
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Physical Properties
Melting Point
94 °C
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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 |
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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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