2-Bromo-5-fluoro-4-nitropyridine

95%

Reagent Code: #79270
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CAS Number 1805578-52-2

science Other reagents with same CAS 1805578-52-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.98 g/mol
Formula C₅H₂BrFN₂O₂
badge Registry Numbers
MDL Number MFCD28740491
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its unique structure, featuring bromine, fluorine, and nitro groups, makes it a versatile building block for constructing complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce functionalized pyridine moieties into target compounds. Additionally, it is used in the development of biologically active compounds, including potential drug candidates for treating diseases like cancer or infections, due to its ability to modulate electronic and steric properties in molecular design. Its application extends to materials science, where it contributes to the synthesis of advanced organic materials with specific electronic or optical properties.

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Test Parameter Specification
Appearance Yellow Liquid
Purity (%) 94.5-100
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿12,816.00
inventory 100mg
10-20 days ฿2,763.00
inventory 250mg
10-20 days ฿4,689.00

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2-Bromo-5-fluoro-4-nitropyridine
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This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its unique structure, featuring bromine, fluorine, and nitro groups, makes it a versatile building block for constructing complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce functionalized pyridine moieties into target compounds. Additionally, it is used in th

This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its unique structure, featuring bromine, fluorine, and nitro groups, makes it a versatile building block for constructing complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce functionalized pyridine moieties into target compounds. Additionally, it is used in the development of biologically active compounds, including potential drug candidates for treating diseases like cancer or infections, due to its ability to modulate electronic and steric properties in molecular design. Its application extends to materials science, where it contributes to the synthesis of advanced organic materials with specific electronic or optical properties.

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