4-(Trimethylsilyl)phenylboronic acid
97%
Reagent
Code: #90523
Alias
4-(Trimethylsilyl)phenylboronic acid
p-Trimethylsilylphenylboronic acid
CAS Number
17865-11-1
blur_circular Chemical Specifications
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Molecular Information
Weight
194.11 g/mol
Formula
C₉H₁₅BO₂Si
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Registry Numbers
MDL Number
MFCD00093348
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Physical Properties
Melting Point
173-178 °C(lit.)
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Storage & Handling
Storage
room temperature
description Product Description
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. Its trimethylsilyl group enhances stability and reactivity, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the synthesis of complex organic molecules, including biaryl compounds, which are essential in drug discovery and material science. Its unique structure also allows for applications in functionalizing surfaces and creating molecular sensors for detecting specific analytes.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Loss on Drying | <=0.5% |
Purity (Neutralization Titration) | 97-100% |
Appearance | White to off-white powder or crystals |
Infrared Spectrum | Conforms to Structure |
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4-(Trimethylsilyl)phenylboronic acid
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. Its trimethylsilyl group enhances stability and reactivity, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the synthesis of complex organic molecules, including biaryl compounds, which are essential in drug discovery and material science. Its unique structure also allows for applications in functionalizing surfaces and creating molecular sensors for detecting specific analytes.
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