4-(Dimethylamino)phenylboronic acid

95%

Reagent Code: #90531
label
Alias 4-(Dimethylamino)phenylboronic acid 4-(N,N-Dimethylamino)phenylboronic acid
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CAS Number 28611-39-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 165 g/mol
Formula C₈H₁₂BNO₂
badge Registry Numbers
MDL Number MFCD01074642
thermostat Physical Properties
Melting Point 227 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of biaryl compounds, which are essential in pharmaceuticals and agrochemicals. Additionally, it is employed in the development of sensors and molecular probes due to its ability to interact with diols and sugars, making it useful in glucose detection and other biochemical applications. Its dimethylamino group further enhances its utility by improving solubility and reactivity in various organic solvents.

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Test Parameter Specification
Purity (LC) 94.5-105.5
Appearance Powder and/or chunks
Infrared Spectrum Conforms to Structure
Proton NMR Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days $127.38
inventory 5g
10-20 days $464.92
inventory 25g
10-20 days $1,501.05
4-(Dimethylamino)phenylboronic acid
This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of biaryl compounds, which are essential in pharmaceuticals and agrochemicals. Additionally, it is employed in the development of sensors and molecular probes due to its ability to interact with diols and sugars, making it useful in glucose detection and other biochemical applications. Its dimethylamino group further enhances its utility by improving solubility and reactivity in various organic solvents.
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