2,4-Dimethylphenylboronic acid

97%

  • Product Code: 89568
  Alias:    2,4-Dimethylphenylboronic acid
  CAS:    55499-44-0
Molecular Weight: 149.98 g./mol Molecular Formula: C₈H₁₁BO₂
EC Number: MDL Number: MFCD02683101
Melting Point: 204-208°C Boiling Point:
Density: Storage Condition: room temperature
Product Description: 2,4-Dimethylphenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its role as a boronic acid derivative makes it a valuable building block in creating biaryl compounds, which are common in drug development. Additionally, it is employed in the preparation of sensors and catalysts due to its ability to interact with various organic and inorganic substrates. Its stability and reactivity under mild conditions further enhance its utility in diverse chemical processes.
Product Specification:
Test Specification
Melting point 206-210
PURITYNEUTRALIZATION TITRATION 96.5-103.5
APPEARANCE WHITE TO OFF-WHITE POWDER OR CHUNKS
INFRARED SPECTRUM Conforms to Structure
PROTON NMR SPECTRUM Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days $16.20
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5.000 10-20 days $49.00
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25.000 10-20 days $212.21
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100.000 10-20 days $768.29
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2,4-Dimethylphenylboronic acid
2,4-Dimethylphenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its role as a boronic acid derivative makes it a valuable building block in creating biaryl compounds, which are common in drug development. Additionally, it is employed in the preparation of sensors and catalysts due to its ability to interact with various organic and inorganic substrates. Its stability and reactivity under mild conditions further enhance its utility in diverse chemical processes.
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