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

98%

Reagent Code: #89186
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CAS Number 1704065-62-2

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Weight 399.39 g/mol
Formula C₁₇H₃₀BNO₅SSi
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MDL Number MFCD28384270
inventory_2 Storage & Handling
Storage  2-8°C

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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 Availability Unit Price Quantity
inventory 1g
10-20 days ฿46,500.00
(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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