3-Aminophenylboronic acid pinacol ester
97%
Reagent
Code: #90192
Alias
3-Aminophenylboronic acid pinacol ester 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
CAS Number
210907-84-9
blur_circular Chemical Specifications
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Molecular Information
Weight
219.09 g/mol
Formula
C₁₂H₁₈BNO₂
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Registry Numbers
MDL Number
MFCD03453668
thermostat
Physical Properties
Melting Point
89-94 °C
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Storage & Handling
Storage
2~8°C
description Product Description
Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to create biaryl compounds, which are essential in pharmaceuticals and agrochemicals. It is also employed in the development of sensors and diagnostic tools due to its ability to bind with diols and sugars, making it useful in glucose detection systems. Additionally, it finds application in materials science for modifying polymers and surfaces to enhance their properties. Its role in the preparation of boron-containing compounds is significant in medicinal chemistry for drug discovery and development.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Carbon | 63.5-68.1 |
Melting point | 89-94 |
Nitrogen | 6.1-6.6 |
Purity (GC) | 96.5-100 |
Appearance | White to yellow to beige powder or crystals |
Infrared Spectrum | Conforms to Structure |
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3-Aminophenylboronic acid pinacol ester
Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to create biaryl compounds, which are essential in pharmaceuticals and agrochemicals. It is also employed in the development of sensors and diagnostic tools due to its ability to bind with diols and sugars, making it useful in glucose detection systems. Additionally, it finds application in materials science for modifying polymers and surfaces to enhance their properties. Its role in the preparation of boron-containing compounds is significant in medicinal chemistry for drug discovery and development.
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