4-(Diphenylamino)phenylboronic acid

98%

Reagent Code: #90538
label
Alias 4-(Diphenylamino)phenylboronic acid Triphenylamine-4-boronic acid
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CAS Number 201802-67-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 289.14 g/mol
Formula C₁₈H₁₆BNO₂
badge Registry Numbers
MDL Number MFCD06798117
thermostat Physical Properties
Melting Point 110-115 °C
inventory_2 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

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿410.00
inventory 5g
10-20 days ฿1,400.00
inventory 25g
10-20 days ฿6,380.00
inventory 100g
10-20 days ฿22,880.00
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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