4-(Diphenylamino)phenylboronic acid
98%
Reagent
Code: #90538
Alias
4-(Diphenylamino)phenylboronic acid Triphenylamine-4-boronic acid
CAS Number
201802-67-7
blur_circular Chemical Specifications
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Molecular Information
Weight
289.14 g/mol
Formula
C₁₈H₁₆BNO₂
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Registry Numbers
MDL Number
MFCD06798117
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Physical Properties
Melting Point
110-115 °C
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Storage & Handling
Storage
room temperature
description Product Description
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts 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 complex organic molecules, including pharmaceuticals and advanced materials. Additionally, it serves as a building block in the development of organic electronic materials, such as organic light-emitting diodes (OLEDs) and organic photovoltaic cells, due to its electron-donating diphenylamino group. Its unique structure also makes it useful in sensor applications, where it can detect specific analytes through boronic acid-diol interactions.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Purity (Neutralization Titration) | 97.5-102.5 |
Appearance | White to off-white powder, crystals and/or chunks |
Infrared Spectrum | Conforms to Structure |
Proton NMR Spectrum | Conforms to Structure |
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4-(Diphenylamino)phenylboronic acid
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts 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 complex organic molecules, including pharmaceuticals and advanced materials. Additionally, it serves as a building block in the development of organic electronic materials, such as organic light-emitting diodes (OLEDs) and organic photovoltaic cells, due to its electron-donating diphenylamino group. Its unique structure also makes it useful in sensor applications, where it can detect specific analytes through boronic acid-diol interactions.
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