2-Methoxy-4-methylnicotinaldehyde

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Reagent Code: #203055
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CAS Number 123506-68-3

science Other reagents with same CAS 123506-68-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 151.16 g/mol
Formula C₈H₉NO₂
badge Registry Numbers
MDL Number MFCD16611506
thermostat Physical Properties
Melting Point 29.5-30 °C
Boiling Point 265.9±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.123±0.06 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of nicotinic receptor modulators. It serves as a building block in agrochemicals for creating novel pesticides due to its reactive aldehyde group and heterocyclic structure. Also employed in organic research for constructing complex nitrogen-containing compounds through condensation and coupling reactions. Its methoxy and methyl substituents enhance electron density, improving reactivity in electrophilic substitution processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,510.00
inventory 1g
10-20 days ฿57,370.00

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2-Methoxy-4-methylnicotinaldehyde
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of nicotinic receptor modulators. It serves as a building block in agrochemicals for creating novel pesticides due to its reactive aldehyde group and heterocyclic structure. Also employed in organic research for constructing complex nitrogen-containing compounds through condensation and coupling reactions. Its methoxy and methyl substituents enhance electron density, improving reactivity in electrophilic substitution p

Used in the synthesis of pharmaceutical intermediates, particularly in the development of nicotinic receptor modulators. It serves as a building block in agrochemicals for creating novel pesticides due to its reactive aldehyde group and heterocyclic structure. Also employed in organic research for constructing complex nitrogen-containing compounds through condensation and coupling reactions. Its methoxy and methyl substituents enhance electron density, improving reactivity in electrophilic substitution processes.

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