(3-(Di-p-tolylamino)phenyl)boronic acid

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Reagent Code: #36637
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CAS Number 1162753-18-5

science Other reagents with same CAS 1162753-18-5

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Weight 317.1900 g/mol
Formula C₂₀H₂₀BNO₂
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Used primarily in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate for creating complex organic molecules. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is utilized in the development of organic light-emitting diodes (OLEDs) due to its electron-donating properties, enhancing the efficiency and performance of these devices. Its role in catalysis and material science further underscores its importance in research and industrial applications.

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inventory 100mg
10-20 days ฿3,339.00

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(3-(Di-p-tolylamino)phenyl)boronic acid
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Used primarily in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate for creating complex organic molecules. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is utilized in the development of organic light-emitting diodes (OLEDs) due to its electron-donating properties, enhancing the efficiency and performa

Used primarily in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate for creating complex organic molecules. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is utilized in the development of organic light-emitting diodes (OLEDs) due to its electron-donating properties, enhancing the efficiency and performance of these devices. Its role in catalysis and material science further underscores its importance in research and industrial applications.

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