2,4-Dimethoxyphenylboronic acid

96%

  • Product Code: 89571
  Alias:    2,4-Dimethoxyphenylboronic acid
  CAS:    133730-34-4
Molecular Weight: 181.98 g./mol Molecular Formula: C₈H₁₁BO₄
EC Number: MDL Number: MFCD01074590
Melting Point: 125-127 °C(lit.) Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: Used as a key reagent in Suzuki-Miyaura cross-coupling reactions to synthesize biaryl compounds, which are important in pharmaceuticals and organic electronics. It serves as a building block in the production of complex organic molecules, particularly in drug discovery and development. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in creating carbon-carbon bonds. Additionally, it is utilized in the synthesis of advanced materials, such as polymers and liquid crystals, due to its ability to introduce methoxy-functionalized phenyl groups. Its stability and reactivity make it a preferred choice in organic synthesis and medicinal chemistry research.
Product Specification:
Test Specification
Melting point 125-129
PURITYHPLC 96-100
PURITYTITRATION WITH NAOH 96.5-103.5
APPEARANCE White to off-white powder
INFRARED SPECTRUM Conforms to Structure
PROTON NMR SPECTRUM Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿390.00
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-
5.000 10-20 days ฿930.00
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-
25.000 10-20 days ฿4,350.00
+
-
100.000 10-20 days ฿17,360.00
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-
2,4-Dimethoxyphenylboronic acid
Used as a key reagent in Suzuki-Miyaura cross-coupling reactions to synthesize biaryl compounds, which are important in pharmaceuticals and organic electronics. It serves as a building block in the production of complex organic molecules, particularly in drug discovery and development. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in creating carbon-carbon bonds. Additionally, it is utilized in the synthesis of advanced materials, such as polymers and liquid crystals, due to its ability to introduce methoxy-functionalized phenyl groups. Its stability and reactivity make it a preferred choice in organic synthesis and medicinal chemistry research.
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