2-Fluoro-6-(3-thienyl)pyridine-3-boronic acid
95%
Reagent
Code: #91643
CAS Number
2225177-72-8
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Molecular Information
Weight
223.0317832 g/mol
Formula
C₉H₇BFNO₂S
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Storage & Handling
Storage
-20℃, sealed and dry
description Product Description
This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the synthesis of heterocyclic compounds, which are valuable in medicinal chemistry for designing drugs with specific biological activities. Its unique structure, combining a thienyl group and a pyridine ring, makes it useful in creating compounds with potential applications in material science, such as organic semiconductors or light-emitting diodes (LEDs).
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2-Fluoro-6-(3-thienyl)pyridine-3-boronic acid
This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the synthesis of heterocyclic compounds, which are valuable in medicinal chemistry for designing drugs with specific biological activities. Its unique structure, combining a thienyl group and a pyridine ring, makes it useful in creating compounds with potential applications in material science, such as organic semiconductors or light-emitting diodes (LEDs).
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