(5-(N,N-Dimethylsulfamoyl)-2-methoxyphenyl)boronic acid
98%
Reagent
Code: #89340
CAS Number
859160-65-9
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Molecular Information
Weight
259.09 g/mol
Formula
C₉H₁₄BNO₅S
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Registry Numbers
MDL Number
MFCD28400388
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Storage & Handling
Storage
2-8°C
description Product Description
This compound is primarily utilized in organic synthesis and pharmaceutical research due to its boronic acid functional group, which is highly effective in Suzuki-Miyaura cross-coupling reactions. These reactions are crucial for forming carbon-carbon bonds, enabling the construction of complex molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its sulfamoyl and methoxy groups enhance its reactivity and selectivity, making it a valuable intermediate in the development of biologically active compounds. Additionally, it is explored in the design of enzyme inhibitors and receptor modulators, particularly in targeting diseases where precise molecular interactions are critical. Its stability and versatility also make it suitable for use in medicinal chemistry for drug discovery and optimization.
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(5-(N,N-Dimethylsulfamoyl)-2-methoxyphenyl)boronic acid
This compound is primarily utilized in organic synthesis and pharmaceutical research due to its boronic acid functional group, which is highly effective in Suzuki-Miyaura cross-coupling reactions. These reactions are crucial for forming carbon-carbon bonds, enabling the construction of complex molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its sulfamoyl and methoxy groups enhance its reactivity and selectivity, making it a valuable intermediate in the development of biologically active compounds. Additionally, it is explored in the design of enzyme inhibitors and receptor modulators, particularly in targeting diseases where precise molecular interactions are critical. Its stability and versatility also make it suitable for use in medicinal chemistry for drug discovery and optimization.
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