3-Acetamidophenylboronic acid
98%
Reagent
Code: #90121
Alias
3-acetamidophenylboronic acid
CAS Number
78887-39-5
blur_circular Chemical Specifications
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Molecular Information
Weight
178.98 g/mol
Formula
C₈H₁₀BNO₃
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Registry Numbers
MDL Number
MFCD00236013
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Physical Properties
Melting Point
135 °C(lit.)
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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 |
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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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