3-Aminophenylboronic acid pinacol ester

97%

Reagent Code: #90192
label
Alias 3-Aminophenylboronic acid pinacol ester 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
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CAS Number 210907-84-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 219.09 g/mol
Formula C₁₂H₁₈BNO₂
badge Registry Numbers
MDL Number MFCD03453668
thermostat Physical Properties
Melting Point 89-94 °C
inventory_2 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

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days $20.05
inventory 5g
10-20 days $73.34
inventory 25g
10-20 days $317.64
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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