(4-(N-Cyclopropylsulfamoyl)- 3-fluorophenyl)boronic acid
98%
Reagent
Code: #89259
CAS Number
1704096-55-8
blur_circular Chemical Specifications
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Molecular Information
Weight
259.06 g/mol
Formula
C₉H₁₁BFNO₄S
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Storage & Handling
Storage
room temperature, dry
description Product Description
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The cyclopropylsulfamoyl group enhances its stability and reactivity, allowing for precise control in the creation of target compounds. Additionally, its fluorine substituent can influence the electronic properties of the resulting molecules, potentially improving their biological activity or chemical stability. This chemical is often employed in the development of new drugs, where its structural features contribute to the optimization of drug candidates.
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(4-(N-Cyclopropylsulfamoyl)- 3-fluorophenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The cyclopropylsulfamoyl group enhances its stability and reactivity, allowing for precise control in the creation of target compounds. Additionally, its fluorine substituent can influence the electronic properties of the resulting molecules, potentially improving their biological activity or chemical stability. This chemical is often employed in the development of new drugs, where its structural features contribute to the optimization of drug candidates.
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