2-Amino-3-methyl-5-nitropyridine

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Reagent Code: #136304
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CAS Number 18344-51-9

science Other reagents with same CAS 18344-51-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 153.14 g/mol
Formula C₆H₇N₃O₂
thermostat Physical Properties
Melting Point 255°C(lit.)
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of certain antihypertensive and anti-inflammatory drugs. It serves as a building block in organic synthesis due to the presence of both amino and nitro functional groups, enabling various derivatization reactions such as acylation, alkylation, or imine formation. Also employed in the development of agrochemicals, such as herbicides and fungicides, where its pyridine-based structure contributes to biological activity. Its derivatives are explored in research for potential use in dyes, fluorescent probes, and materials science applications like luminescent materials or sensors, owing to their electron-donating and accepting properties.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿960.00
inventory 100g
10-20 days ฿3,840.00

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2-Amino-3-methyl-5-nitropyridine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of certain antihypertensive and anti-inflammatory drugs. It serves as a building block in organic synthesis due to the presence of both amino and nitro functional groups, enabling various derivatization reactions such as acylation, alkylation, or imine formation. Also employed in the development of agrochemicals, such as herbicides and fungicides, where its pyridine-based structure contributes to biological activity.
Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of certain antihypertensive and anti-inflammatory drugs. It serves as a building block in organic synthesis due to the presence of both amino and nitro functional groups, enabling various derivatization reactions such as acylation, alkylation, or imine formation. Also employed in the development of agrochemicals, such as herbicides and fungicides, where its pyridine-based structure contributes to biological activity. Its derivatives are explored in research for potential use in dyes, fluorescent probes, and materials science applications like luminescent materials or sensors, owing to their electron-donating and accepting properties.
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