(4-((tert-Butyldimethylsilyl)oxy)-2-chlorophenyl)boronic acid
98%
Reagent
Code: #89781
CAS Number
412343-21-6
blur_circular Chemical Specifications
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Molecular Information
Weight
286.64 g/mol
Formula
C₁₂H₂₀BClO₃Si
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Registry Numbers
MDL Number
MFCD04037223
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Storage & Handling
Storage
2-8°C
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 boronic acid derivative, enabling the formation of carbon-carbon bonds, which is essential in constructing complex organic molecules. The tert-butyldimethylsilyl (TBDMS) group acts as a protecting group for the hydroxyl functionality, ensuring selective reactivity during the synthesis process. This compound is valuable in pharmaceutical research and development, where it aids in the creation of drug intermediates and biologically active compounds. Its stability and reactivity make it a useful tool in advanced chemical transformations.
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