2, 6-Dimethyl-4-nitropyridine

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Reagent Code: #177941
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CAS Number 4913-57-9

science Other reagents with same CAS 4913-57-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 152.15 g/mol
Formula C₇H₈N₂O₂
badge Registry Numbers
MDL Number MFCD00234324
thermostat Physical Properties
Melting Point 47℃
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor agonists and other central nervous system agents. It serves as a building block in agrochemicals for the production of certain herbicides and insecticides due to its stable pyridine ring structure. Also employed in research laboratories for the preparation of functionalized pyridine derivatives used in catalysis and material science. Its nitro group allows for further chemical modifications, enabling the introduction of amino or other functional groups through reduction or substitution reactions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿850.00
inventory 1g
10-20 days ฿3,300.00
inventory 5g
10-20 days ฿14,210.00

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2, 6-Dimethyl-4-nitropyridine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor agonists and other central nervous system agents. It serves as a building block in agrochemicals for the production of certain herbicides and insecticides due to its stable pyridine ring structure. Also employed in research laboratories for the preparation of functionalized pyridine derivatives used in catalysis and material science. Its nitro group allows for further chemical modifications,

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor agonists and other central nervous system agents. It serves as a building block in agrochemicals for the production of certain herbicides and insecticides due to its stable pyridine ring structure. Also employed in research laboratories for the preparation of functionalized pyridine derivatives used in catalysis and material science. Its nitro group allows for further chemical modifications, enabling the introduction of amino or other functional groups through reduction or substitution reactions.

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