4-Methoxy-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

98%

  • Product Code: 119485
  CAS:    758699-74-0
Molecular Weight: 235.09 g./mol Molecular Formula: C₁₂H₁₈BNO₃
EC Number: MDL Number: MFCD07367561
Melting Point: Boiling Point: 346.7°C at 760 mmHg
Density: Storage Condition: 2-8°C, store under inert gas
Product Description: This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research and development. Its boronate ester group enables efficient coupling with aryl or vinyl halides, making it valuable for creating carbon-carbon bonds. This compound is often employed in the synthesis of biologically active compounds, including potential drug candidates, due to its stability and reactivity under mild conditions. Additionally, it finds use in material science for designing organic electronic materials and polymers. Its versatility in various synthetic pathways highlights its importance in advancing chemical and medicinal research.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.050 10-20 days Ft6,787.69
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0.100 10-20 days Ft8,436.13
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0.250 10-20 days Ft11,151.20
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4-Methoxy-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research and development. Its boronate ester group enables efficient coupling with aryl or vinyl halides, making it valuable for creating carbon-carbon bonds. This compound is often employed in the synthesis of biologically active compounds, including potential drug candidates, due to its stability and reactivity under mild conditions. Additionally, it finds use in material science for designing organic electronic materials and polymers. Its versatility in various synthetic pathways highlights its importance in advancing chemical and medicinal research.
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