[4-[Bis(4-methoxyphenyl)amino]phenyl]boronic Acid

98%, containing different amounts of acid anhydride

  • Product Code: 77825
  CAS:    201802-29-1
Molecular Weight: 349.19 g./mol Molecular Formula: C₂₀H₂₀BNO₄
EC Number: MDL Number: MFCD28385171
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: This compound is primarily utilized in organic synthesis and materials science due to its unique boronic acid functional group, which enables it to participate in Suzuki-Miyaura cross-coupling reactions. These reactions are widely employed in the construction of complex organic molecules, particularly in the pharmaceutical industry for the synthesis of drug candidates. Additionally, its structure, featuring methoxy-substituted aromatic rings, makes it suitable for applications in optoelectronics, such as in the development of organic light-emitting diodes (OLEDs) or photovoltaic materials, where it can contribute to charge transport properties. Its ability to interact with diols also makes it useful in sensor technologies, particularly for detecting sugars or other biomolecules.
Product Specification:
Test Specification
APPEARANCE White - Very pale yellow Solid
PURITY 98-100
Infrared spectrum Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.200 10-20 days ฿1,980.00
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1.000 10-20 days ฿5,470.00
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[4-[Bis(4-methoxyphenyl)amino]phenyl]boronic Acid
This compound is primarily utilized in organic synthesis and materials science due to its unique boronic acid functional group, which enables it to participate in Suzuki-Miyaura cross-coupling reactions. These reactions are widely employed in the construction of complex organic molecules, particularly in the pharmaceutical industry for the synthesis of drug candidates. Additionally, its structure, featuring methoxy-substituted aromatic rings, makes it suitable for applications in optoelectronics, such as in the development of organic light-emitting diodes (OLEDs) or photovoltaic materials, where it can contribute to charge transport properties. Its ability to interact with diols also makes it useful in sensor technologies, particularly for detecting sugars or other biomolecules.
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