4-(Dimethylcarbamoyl)benzeneboronic acid

97%

Reagent Code: #90534
label
Alias 4-(Dimethylcarbamoyl)phenylboronic acid 4-(N,N-Dimethylformamide)phenylboronic acid
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CAS Number 405520-68-5

science Other reagents with same CAS 405520-68-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.01 g/mol
Formula C₉H₁₂BNO₃
badge Registry Numbers
MDL Number MFCD02258943
thermostat Physical Properties
Melting Point 130-136°C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boronic acid reagent, enabling the formation of carbon-carbon bonds between aryl or vinyl boronic acids and aryl or vinyl halides. This reaction is widely employed in the pharmaceutical industry for the synthesis of complex molecules, including drug intermediates and active pharmaceutical ingredients (APIs). Additionally, it finds applications in material science for the development of organic electronic materials, such as polymers and small molecules used in organic light-emitting diodes (OLEDs) and other optoelectronic devices. Its stability and reactivity make it a valuable tool in research and industrial processes.

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Test Parameter Specification
Purity (Titration by NaOH) 97-100
Appearance White to yellow powder or crystals
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 ฿620.00
inventory 5g
10-20 days ฿1,700.00
inventory 25g
10-20 days ฿5,790.00

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4-(Dimethylcarbamoyl)benzeneboronic acid
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boronic acid reagent, enabling the formation of carbon-carbon bonds between aryl or vinyl boronic acids and aryl or vinyl halides. This reaction is widely employed in the pharmaceutical industry for the synthesis of complex molecules, including drug intermediates and active pharmaceutical ingredients (APIs). Additionally, it finds applications in material science for the devel

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boronic acid reagent, enabling the formation of carbon-carbon bonds between aryl or vinyl boronic acids and aryl or vinyl halides. This reaction is widely employed in the pharmaceutical industry for the synthesis of complex molecules, including drug intermediates and active pharmaceutical ingredients (APIs). Additionally, it finds applications in material science for the development of organic electronic materials, such as polymers and small molecules used in organic light-emitting diodes (OLEDs) and other optoelectronic devices. Its stability and reactivity make it a valuable tool in research and industrial processes.

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