4-Isopropylsulfonylbenzeneboronic acid

97%

Reagent Code: #90570
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CAS Number 850567-98-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.07 g/mol
Formula C₉H₁₃BO₄S
badge Registry Numbers
MDL Number MFCD06659866
thermostat Physical Properties
Melting Point 126-128
inventory_2 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.

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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

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿8,000.00
inventory 250mg
10-20 days ฿580.00
inventory 1g
10-20 days ฿1,660.00
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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