(4-((4-((tert-Butyldimethylsilyl)oxy)piperidin-1-yl)sulfonyl)phenyl)boronic acid

98%

  • Product Code: 89186
  CAS:    1704065-62-2
Molecular Weight: 399.39 g./mol Molecular Formula: C₁₇H₃₀BNO₅SSi
EC Number: MDL Number: MFCD28384270
Melting Point: Boiling Point:
Density: Storage Condition:  2-8°C
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 boronic acid derivative, enabling the formation of carbon-carbon bonds, which is essential in constructing complex organic molecules. Its tert-butyldimethylsilyl (TBDMS) protected hydroxyl group enhances stability during reactions, making it suitable for multi-step synthetic processes. It is often employed in pharmaceutical research and development for creating drug intermediates or active pharmaceutical ingredients (APIs). Additionally, its sulfonyl group can act as a directing group or participate in further functionalization, expanding its utility in medicinal chemistry and material science.
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Size (g) Availability Price Quantity
1.000 10-20 days $1,931.10
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(4-((4-((tert-Butyldimethylsilyl)oxy)piperidin-1-yl)sulfonyl)phenyl)boronic acid
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a boronic acid derivative, enabling the formation of carbon-carbon bonds, which is essential in constructing complex organic molecules. Its tert-butyldimethylsilyl (TBDMS) protected hydroxyl group enhances stability during reactions, making it suitable for multi-step synthetic processes. It is often employed in pharmaceutical research and development for creating drug intermediates or active pharmaceutical ingredients (APIs). Additionally, its sulfonyl group can act as a directing group or participate in further functionalization, expanding its utility in medicinal chemistry and material science.
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