5-Bromo-3-methoxy-2-nitropyridine

98%

Reagent Code: #145443
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CAS Number 152684-26-9

science Other reagents with same CAS 152684-26-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.02 g/mol
Formula C₆H₅BrN₂O₃
thermostat Physical Properties
Melting Point 112°C
Boiling Point 334.6°C
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 kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amine groups. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its electron-deficient pyridine core.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,160.00
inventory 5g
10-20 days ฿5,720.00

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5-Bromo-3-methoxy-2-nitropyridine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amine groups. Also utilized in agrochemical research for designing novel pesticides and herbicides due

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amine groups. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its electron-deficient pyridine core.

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