2,5-Dibromopyridine 1-oxide

≥97%

Reagent Code: #177635
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CAS Number 20734-22-9

science Other reagents with same CAS 20734-22-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.89 g/mol
Formula C₅H₃Br₂NO
badge Registry Numbers
MDL Number MFCD06200199
thermostat Physical Properties
Boiling Point 387.6±22.0 °C(Predicted)
inventory_2 Storage & Handling
Density 2.15±0.1 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of pyridine-based active ingredients. Its bromine groups allow for selective cross-coupling reactions, making it valuable in constructing complex molecules via palladium-catalyzed reactions like Suzuki or Heck couplings. Also employed in the preparation of functionalized pyridine derivatives for use in materials science and ligand design. The N-oxide functionality enhances reactivity and directs substitution patterns, enabling precise control in synthetic pathways.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿21,170.00
inventory 10g
10-20 days ฿32,610.00

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2,5-Dibromopyridine 1-oxide
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of pyridine-based active ingredients. Its bromine groups allow for selective cross-coupling reactions, making it valuable in constructing complex molecules via palladium-catalyzed reactions like Suzuki or Heck couplings. Also employed in the preparation of functionalized pyridine derivatives for use in materials science and ligand design. The N-oxide functionality enhances reactivity and directs

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of pyridine-based active ingredients. Its bromine groups allow for selective cross-coupling reactions, making it valuable in constructing complex molecules via palladium-catalyzed reactions like Suzuki or Heck couplings. Also employed in the preparation of functionalized pyridine derivatives for use in materials science and ligand design. The N-oxide functionality enhances reactivity and directs substitution patterns, enabling precise control in synthetic pathways.

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