2-Bromo-4-chloro-3-nitropyridine

≥95%

Reagent Code: #43234
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CAS Number 1261732-45-9

science Other reagents with same CAS 1261732-45-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.44 g/mol
Formula C₅H₂BrClN₂O₂
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

2-Bromo-4-chloro-3-nitropyridine is primarily used as a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure allows for various chemical transformations, making it valuable for creating complex molecules. It is often employed in cross-coupling reactions to form carbon-carbon or carbon-heteroatom bonds, which are essential in drug discovery processes. Additionally, it serves as a building block for synthesizing pyridine derivatives that exhibit biological activity, such as antimicrobial or anti-inflammatory agents. Its halogen and nitro groups provide reactive sites for further functionalization, enabling the production of diverse compounds with potential applications in medicinal chemistry and material science.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,579.00
inventory 250mg
10-20 days ฿13,158.00

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2-Bromo-4-chloro-3-nitropyridine
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2-Bromo-4-chloro-3-nitropyridine is primarily used as a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure allows for various chemical transformations, making it valuable for creating complex molecules. It is often employed in cross-coupling reactions to form carbon-carbon or carbon-heteroatom bonds, which are essential in drug discovery processes. Additionally, it serves as a building block for synthesizing pyridine derivative

2-Bromo-4-chloro-3-nitropyridine is primarily used as a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure allows for various chemical transformations, making it valuable for creating complex molecules. It is often employed in cross-coupling reactions to form carbon-carbon or carbon-heteroatom bonds, which are essential in drug discovery processes. Additionally, it serves as a building block for synthesizing pyridine derivatives that exhibit biological activity, such as antimicrobial or anti-inflammatory agents. Its halogen and nitro groups provide reactive sites for further functionalization, enabling the production of diverse compounds with potential applications in medicinal chemistry and material science.

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