Pyridine-4-Boronic Acid Hydrochloride

≥98%

Reagent Code: #91183
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CAS Number 913835-65-1

science Other reagents with same CAS 913835-65-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 159.38 g/mol
Formula C₅H₇BNO₂Cl
inventory_2 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.

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Test Parameter Specification
Appearance White to Off-White Powder or Crystals
Purity (%) 98.0-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,071.00
inventory 1g
10-20 days ฿333.00
inventory 25g
10-20 days ฿3,744.00

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Pyridine-4-Boronic Acid Hydrochloride
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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

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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