3-Methoxy-2-nitropyridine

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Reagent Code: #204781
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Alias 2-nitro-3-methoxypyridine
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CAS Number 20265-37-6

science Other reagents with same CAS 20265-37-6

blur_circular Chemical Specifications

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Weight 154.12 g/mol
Formula C₆H₆N₂O₃
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MDL Number MFCD00222276
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) where pyridine derivatives are key structural components. Its functional groups enable selective transformations, making it valuable in constructing complex heterocyclic systems. Commonly employed in research settings for nitration and methoxylation studies, it supports the creation of agrochemicals, dyes, and specialty chemicals. Its reactivity profile allows for use in cross-coupling reactions and nucleophilic substitutions, facilitating the introduction of nitrogen-containing rings in target molecules.

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Size Availability Unit Price Quantity
inventory 100g
10-20 days ฿2,000.00
inventory 500g
10-20 days ฿9,800.00
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3-Methoxy-2-nitropyridine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where pyridine derivatives are key structural components. Its functional groups enable selective transformations, making it valuable in constructing complex heterocyclic systems. Commonly employed in research settings for nitration and methoxylation studies, it supports the creation of agrochemicals, dyes, and specialty chemicals. Its reactivity profile allows for use i

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where pyridine derivatives are key structural components. Its functional groups enable selective transformations, making it valuable in constructing complex heterocyclic systems. Commonly employed in research settings for nitration and methoxylation studies, it supports the creation of agrochemicals, dyes, and specialty chemicals. Its reactivity profile allows for use in cross-coupling reactions and nucleophilic substitutions, facilitating the introduction of nitrogen-containing rings in target molecules.

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