(2-((tert-Butyldimethylsilyl)oxy)phenyl)boronic acid
98%
Reagent
Code: #36316
CAS Number
929277-63-4
blur_circular Chemical Specifications
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Molecular Information
Weight
252.19 g/mol
Formula
C₁₂H₂₁BO₃Si
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Registry Numbers
MDL Number
MFCD18783118
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Physical Properties
Boiling Point
327.3±44.0°C at 760 mmHg
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Storage & Handling
Storage
2-8°C, store under inert gas
description Product Description
(2-((tert-Butyldimethylsilyl)oxy)phenyl)boronic acid is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical and materials science industries to form carbon-carbon bonds, enabling the synthesis of complex organic molecules. The tert-butyldimethylsilyl (TBDMS) protecting group in the compound enhances stability and selectivity during reactions, making it valuable for constructing intermediates in drug development and fine chemical production. Additionally, its boronic acid moiety allows for efficient conjugation with various organic substrates, facilitating the creation of biaryl compounds, which are essential in agrochemicals, polymers, and advanced materials.
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