2-Methoxy-3-nitropyridine

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Reagent Code: #205354
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CAS Number 20265-35-4

science Other reagents with same CAS 20265-35-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 154.12 g/mol
Formula C₆H₆N₂O₃
badge Registry Numbers
MDL Number MFCD00023459
thermostat Physical Properties
Melting Point 53-55°C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) involving pyridine derivatives. Its structure allows for selective functionalization, making it valuable in creating complex heterocyclic compounds. Commonly employed in reactions where nitro group reduction or methoxy group displacement is required. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its electron-deficient aromatic ring, which enhances binding to biological targets. Suitable for use in cross-coupling reactions and nucleophilic aromatic substitution under controlled conditions.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿150.00
inventory 5g
10-20 days ฿390.00
inventory 25g
10-20 days ฿781.00
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2-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) involving pyridine derivatives. Its structure allows for selective functionalization, making it valuable in creating complex heterocyclic compounds. Commonly employed in reactions where nitro group reduction or methoxy group displacement is required. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its electron-deficient aromatic
Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) involving pyridine derivatives. Its structure allows for selective functionalization, making it valuable in creating complex heterocyclic compounds. Commonly employed in reactions where nitro group reduction or methoxy group displacement is required. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its electron-deficient aromatic ring, which enhances binding to biological targets. Suitable for use in cross-coupling reactions and nucleophilic aromatic substitution under controlled conditions.
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