3-Bromopyridine-4-boronic acid

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Reagent Code: #90234
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CAS Number 458532-99-5

science Other reagents with same CAS 458532-99-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.81 g/mol
Formula C₅H₅BBrNO₂
badge Registry Numbers
MDL Number MFCD06801678
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

3-Bromopyridine-4-boronic acid is widely used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. 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 functional group, enabling the creation of complex molecules with high precision. Additionally, it serves as a building block in medicinal chemistry for designing drug candidates, especially in the development of heterocyclic compounds. Its versatility also extends to material science, where it contributes to the synthesis of organic electronic materials and polymers.

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Test Parameter Specification
Appearance Light Yellow Solid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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inventory 1g
10-20 days ฿18,690.00

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3-Bromopyridine-4-boronic acid
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3-Bromopyridine-4-boronic acid is widely used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. 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 functional group, enabling the creation of complex molecules with high precision. Additionally, it serves as a building block in medicinal chemistry for designing drug candi

3-Bromopyridine-4-boronic acid is widely used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. 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 functional group, enabling the creation of complex molecules with high precision. Additionally, it serves as a building block in medicinal chemistry for designing drug candidates, especially in the development of heterocyclic compounds. Its versatility also extends to material science, where it contributes to the synthesis of organic electronic materials and polymers.

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