2-Chloropyridine-3-boronic acid

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Reagent Code: #89799
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Alias 2-Chloropyridine-3-boronic acid
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CAS Number 381248-04-0

science Other reagents with same CAS 381248-04-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 157.36 g/mol
Formula C₅H₅BClNO₂
badge Registry Numbers
MDL Number MFCD03094997
thermostat Physical Properties
Melting Point 160°C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

2-Chloropyridine-3-boronic acid is widely used as a building block in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and materials. The compound's boronic acid group facilitates its role as a key intermediate in creating biaryl structures, which are common in drug development. Additionally, it is utilized in the preparation of heterocyclic compounds, which are significant in medicinal chemistry due to their biological activity. Its applications also extend to material science, where it contributes to the development of organic electronic materials and polymers.

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Test Parameter Specification
Melting point 115-120
Purity (HPLC) 97-100
Appearance White to light yellow powder
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿290.00
inventory 1g
10-20 days ฿530.00
inventory 25g
10-20 days ฿6,160.00
inventory 5g
10-20 days ฿1,480.00

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2-Chloropyridine-3-boronic acid
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2-Chloropyridine-3-boronic acid is widely used as a building block in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and materials. The compound's boronic acid group facilitates its role as a key intermediate in creating biaryl structures, which are common in drug development. Additionally, it is utilized in the preparation

2-Chloropyridine-3-boronic acid is widely used as a building block in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and materials. The compound's boronic acid group facilitates its role as a key intermediate in creating biaryl structures, which are common in drug development. Additionally, it is utilized in the preparation of heterocyclic compounds, which are significant in medicinal chemistry due to their biological activity. Its applications also extend to material science, where it contributes to the development of organic electronic materials and polymers.

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