2-Bromo-6-methoxy-3-nitropyridine

95%

Reagent Code: #146245
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CAS Number 344296-05-5

science Other reagents with same CAS 344296-05-5

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Weight 233.02 g/mol
Formula C₆H₅BrN₂O₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) targeting central nervous system disorders and anti-inflammatory agents. Its structure allows for selective functionalization, making it valuable in constructing complex pyridine-based molecules. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its electron-deficient ring system that enhances binding to biological targets.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿800.00
inventory 5g
10-20 days ฿3,600.00
inventory 25g
10-20 days ฿13,150.00

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2-Bromo-6-methoxy-3-nitropyridine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) targeting central nervous system disorders and anti-inflammatory agents. Its structure allows for selective functionalization, making it valuable in constructing complex pyridine-based molecules. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups. Also utilized in agrochemical research for designing
Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) targeting central nervous system disorders and anti-inflammatory agents. Its structure allows for selective functionalization, making it valuable in constructing complex pyridine-based molecules. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its electron-deficient ring system that enhances binding to biological targets.
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