4-(1-Hydroxy-1-methylethyl)thiophene-3-boronic acid pinacol ester

95%

  • Product Code: 90320
  CAS:    2223031-70-5
Molecular Weight: 286.19532 g./mol Molecular Formula: C₁₃H₂₃BO₄S
EC Number: MDL Number:
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Density: Storage Condition: -20°C, sealed, dry
Product Description: This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic ester functional group makes it a valuable building block for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. It is often employed in the synthesis of thiophene derivatives, which are key components in materials science, including organic semiconductors and conductive polymers. Additionally, it serves as an intermediate in the development of biologically active compounds, contributing to drug discovery and medicinal chemistry research.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.025 10-20 days £2,171.23
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0.100 10-20 days £6,445.85
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4-(1-Hydroxy-1-methylethyl)thiophene-3-boronic acid pinacol ester
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic ester functional group makes it a valuable building block for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. It is often employed in the synthesis of thiophene derivatives, which are key components in materials science, including organic semiconductors and conductive polymers. Additionally, it serves as an intermediate in the development of biologically active compounds, contributing to drug discovery and medicinal chemistry research.
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