4-(tert-Butyldimethylsilyloxy)phenylboronic acid

97%

Reagent Code: #90536
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Alias 4-(tert-Butyldimethylsilyloxy)phenylboronic acid
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CAS Number 159191-56-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.19 g/mol
Formula C₁₂H₂₁BO₃Si
badge Registry Numbers
MDL Number MFCD03093888
thermostat Physical Properties
Melting Point 194-198 °C(lit.);207℃
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, especially in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The tert-butyldimethylsilyloxy group provides protection for the phenolic hydroxyl group, allowing selective reactions to occur at the boronic acid site. This compound is valuable in the development of bioactive compounds, including drug candidates, due to its ability to form carbon-carbon bonds efficiently. Additionally, it is utilized in the preparation of organic electronic materials, where precise molecular architecture is required.

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Test Parameter Specification
Purity (Neutralization Titration) 97-103
Appearance White to off-white powder
Infrared Spectrum Conforms to Structure
Proton NMR Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿370.00
inventory 1g
10-20 days ฿1,220.00
inventory 5g
10-20 days ฿5,500.00
inventory 25g
10-20 days ฿20,580.00
4-(tert-Butyldimethylsilyloxy)phenylboronic acid
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, especially in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The tert-butyldimethylsilyloxy group provides protection for the phenolic hydroxyl group, allowing selective reactions to occur at the boronic acid site. This compound is valuable in the development of bioactive compounds, including drug candidates, due to its ability to form carbon-carbon bonds efficiently. Additionally, it is utilized in the preparation of organic electronic materials, where precise molecular architecture is required.
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