Pyridine-4-Boronic Acid Hydrochloride
≥98%
Reagent
Code: #91183
CAS Number
913835-65-1
blur_circular Chemical Specifications
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Molecular Information
Weight
159.38 g/mol
Formula
C₅H₇BNO₂Cl
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Storage & Handling
Storage
room temperature, dry
description Product Description
Pyridine-4-Boronic Acid Hydrochloride is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, enabling the coupling of aryl or vinyl halides with arylboronic acids to create complex organic molecules.
In medicinal chemistry, it serves as a building block for designing and synthesizing drug candidates, especially in the development of kinase inhibitors and other bioactive compounds. Its pyridine moiety contributes to the molecule's ability to interact with biological targets, enhancing its utility in drug discovery.
Additionally, it finds applications in material science, where it is used to modify surfaces or create functionalized polymers. Its ability to form stable covalent bonds makes it suitable for developing sensors, catalysts, and other advanced materials. Overall, its versatility and reactivity make it a crucial component in various chemical and industrial processes.
shopping_cart Available Sizes & Pricing
Pyridine-4-Boronic Acid Hydrochloride
Pyridine-4-Boronic Acid Hydrochloride is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, enabling the coupling of aryl or vinyl halides with arylboronic acids to create complex organic molecules.
In medicinal chemistry, it serves as a building block for designing and synthesizing drug candidates, especially in the development of kinase inhibitors and other bioactive compounds. Its pyridine moiety contributes to the molecule's ability to interact with biological targets, enhancing its utility in drug discovery.
Additionally, it finds applications in material science, where it is used to modify surfaces or create functionalized polymers. Its ability to form stable covalent bonds makes it suitable for developing sensors, catalysts, and other advanced materials. Overall, its versatility and reactivity make it a crucial component in various chemical and industrial processes.
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