3-Bromo-2-methoxy-5-nitropyridine

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Reagent Code: #151312
label
Alias 2-Methoxy-3-Bromo-5-nitropyridine
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CAS Number 15862-50-7

science Other reagents with same CAS 15862-50-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.02 g/mol
Formula C₆H₅BrN₂O₃
badge Registry Numbers
MDL Number MFCD06659517
thermostat Physical Properties
Melting Point 89 °C
Boiling Point 285 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, inert gas

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-infective agents. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki and Buchwald-Hartwig aminations to form carbon-carbon and carbon-nitrogen bonds. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its electron-deficient pyridine core. Suitable for use in medicinal chemistry for lead optimization and scaffold modification.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,090.00
inventory 10g
10-20 days ฿2,150.00
inventory 25g
10-20 days ฿5,360.00
inventory 100g
10-20 days ฿18,550.00

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3-Bromo-2-methoxy-5-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-infective agents. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki and Buchwald-Hartwig aminations to form carbon-carbon and carbon-nitrogen bonds. Also utilized in agrochemical research for
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-infective agents. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki and Buchwald-Hartwig aminations to form carbon-carbon and carbon-nitrogen bonds. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its electron-deficient pyridine core. Suitable for use in medicinal chemistry for lead optimization and scaffold modification.
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