(2-((tert-Butyldimethylsilyl)oxy)phenyl)boronic acid

98%

Reagent Code: #36316
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CAS Number 929277-63-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.19 g/mol
Formula C₁₂H₂₁BO₃Si
badge Registry Numbers
MDL Number MFCD18783118
thermostat Physical Properties
Boiling Point 327.3±44.0°C at 760 mmHg
inventory_2 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.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,548.00
inventory 100mg
10-20 days ฿675.00

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