(((Methylazanediyl)bis(methylene))bis(4,1-phenylene))diboronic acid

98%

Reagent Code: #88969
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CAS Number 1704074-22-5

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Weight 298.94 g/mol
Formula C₁₅H₁₉B₂NO₄
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MDL Number MFCD28805766
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 key reagent for the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. As a diboronic acid derivative, its boronic acid groups enable coupling with aryl halides, facilitating the synthesis of extended biaryl systems. This makes it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of organic electronic materials, such as organic light-emitting diodes (OLEDs) and semiconductors, due to its ability to create conjugated systems with precise structural control. Its application also extends to the preparation of polymers and dendrimers, where it aids in creating well-defined architectures.

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inventory 500mg
10-20 days ฿37,260.00

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(((Methylazanediyl)bis(methylene))bis(4,1-phenylene))diboronic acid
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. As a diboronic acid derivative, its boronic acid groups enable coupling with aryl halides, facilitating the synthesis of extended biaryl systems. This makes it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is empl

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. As a diboronic acid derivative, its boronic acid groups enable coupling with aryl halides, facilitating the synthesis of extended biaryl systems. This makes it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of organic electronic materials, such as organic light-emitting diodes (OLEDs) and semiconductors, due to its ability to create conjugated systems with precise structural control. Its application also extends to the preparation of polymers and dendrimers, where it aids in creating well-defined architectures.

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