(4-((4-((tert-Butyldiphenylsilyl)oxy)piperidin- 1-yl)methyl)phenyl)boronic acid

98%

Reagent Code: #89188
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CAS Number 1704082-69-8

science Other reagents with same CAS 1704082-69-8

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Weight 473.49 g/mol
Formula C₂₈H₃₆BNO₃Si
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The tert-butyldiphenylsilyl (TBDPS) group serves as a protective moiety for hydroxyl groups, ensuring selective reactivity during multi-step synthetic processes. Its application extends to the development of bioactive compounds and materials science, where precise molecular construction is essential.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿29,230.00
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(4-((4-((tert-Butyldiphenylsilyl)oxy)piperidin- 1-yl)methyl)phenyl)boronic acid
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This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The tert-butyldiphenylsilyl (TBDPS) group serves as a protective moiety for hydroxyl groups, ensuring selective reactivity during multi-step synthetic processes. Its application extends to the development of bioactive compounds and materials science, where precise molecular construction is essential.
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