4-Isopropylsulfonylbenzeneboronic acid
97%
Reagent
Code: #90570
CAS Number
850567-98-5
blur_circular Chemical Specifications
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Molecular Information
Weight
228.07 g/mol
Formula
C₉H₁₃BO₄S
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Registry Numbers
MDL Number
MFCD06659866
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Physical Properties
Melting Point
126-128
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Storage & Handling
Storage
room temperature
description Product Description
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules, such as pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates efficient coupling with aryl or vinyl halides in the presence of a palladium catalyst. Additionally, it is employed in the development of sensors and diagnostic tools due to its ability to interact with diols and other biomolecules, making it valuable in biochemical research and medical applications.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Carbon by Elemental Analysis | 45.4-47.9% |
Melting point | 126-128 |
Oxygen by Elemental Analysis | 26.7-28.5% |
Purity (HPLC) | 97-100% |
Sulfur by Elemental Analysis | 13.2-14.5 |
Proton NMR Spectrum | Conforms to Structure |
Appearance | White to off-white solid |
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4-Isopropylsulfonylbenzeneboronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules, such as pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates efficient coupling with aryl or vinyl halides in the presence of a palladium catalyst. Additionally, it is employed in the development of sensors and diagnostic tools due to its ability to interact with diols and other biomolecules, making it valuable in biochemical research and medical applications.
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