2-Bromo-5-methyl-3-nitropyridine

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Reagent Code: #145168
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CAS Number 23056-46-4

science Other reagents with same CAS 23056-46-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.02 g/mol
Formula C₆H₅BrN₂O₂
thermostat Physical Properties
Boiling Point 276.7°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 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 heterocyclic compounds. Also employed in agrochemical research for developing novel pesticides and herbicides due to its reactivity and stability in multi-step reactions. Commonly utilized in cross-coupling reactions such as Suzuki and Buchwald-Hartwig aminations to form carbon-carbon and carbon-nitrogen bonds in advanced organic synthesis.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿1,910.00
inventory 100g
10-20 days ฿7,610.00
inventory 500g
10-20 days ฿22,730.00

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2-Bromo-5-methyl-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 heterocyclic compounds. Also employed in agrochemical research for developing novel pesticides and herbicides due to its reactivity and stability in multi-step reactions. Commonly utilized in cross-coup

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 heterocyclic compounds. Also employed in agrochemical research for developing novel pesticides and herbicides due to its reactivity and stability in multi-step reactions. Commonly utilized in cross-coupling reactions such as Suzuki and Buchwald-Hartwig aminations to form carbon-carbon and carbon-nitrogen bonds in advanced organic synthesis.

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