4-(tert-Butyldimethylsilyloxy)phenylboronic acid
97%
Reagent
Code: #90536
Alias
4-(tert-Butyldimethylsilyloxy)phenylboronic acid
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.
format_list_bulleted Product Specification
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
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.
Mechanism | - |
Appearance | - |
Longevity | - |
Strength | - |
Storage | - |
Shelf Life | - |
Allergen(s) | - |
Dosage (Range) | - |
Recommended Dosage | - |
Dosage (Per Day) | - |
Recommended Dosage (Per Day) | - |
Mix Method | - |
Heat Resistance | - |
Stable in pH range | - |
Solubility | - |
Product Types | - |
INCI | - |
Purchase History for
Loading purchase history...
Cart
No products
Subtotal:
฿0.00
Total
฿0.00
THB