(4-((4-((tert-Butyldimethylsilyl)oxy)piperidin-1-yl)sulfonyl)phenyl)boronic acid
98%
Reagent
Code: #89186
CAS Number
1704065-62-2
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Molecular Information
Weight
399.39 g/mol
Formula
C₁₇H₃₀BNO₅SSi
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Registry Numbers
MDL Number
MFCD28384270
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Storage & Handling
Storage
2-8°C
description 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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(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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