(4-(N-Cyclopropylsulfamoyl)- 3-fluorophenyl)boronic acid

98%

Reagent Code: #89259
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CAS Number 1704096-55-8

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Weight 259.06 g/mol
Formula C₉H₁₁BFNO₄S
inventory_2 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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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿50,210.00
(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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