2,3-Dimethoxy-6-methylpyridine

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Reagent Code: #131472
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CAS Number 861019-58-1

science Other reagents with same CAS 861019-58-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 153.18 g/mol
Formula C₈H₁₁NO₂
badge Registry Numbers
MDL Number MFCD11857663
thermostat Physical Properties
Boiling Point 198.6±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.042±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of certain antipsychotic and antidepressant drugs. It serves as a building block in organic reactions where the methoxy and methyl groups aid in directing substitution patterns during drug development. Also employed in the preparation of agrochemicals and specialty heterocyclic compounds due to its stable pyridine ring and reactive sites. Its derivatives are explored in research for potential bioactive molecules and catalysts in asymmetric synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,450.00
inventory 250mg
10-20 days ฿24,660.00

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2,3-Dimethoxy-6-methylpyridine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of certain antipsychotic and antidepressant drugs. It serves as a building block in organic reactions where the methoxy and methyl groups aid in directing substitution patterns during drug development. Also employed in the preparation of agrochemicals and specialty heterocyclic compounds due to its stable pyridine ring and reactive sites. Its derivatives are explored in research for potential bioactive molecules a

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of certain antipsychotic and antidepressant drugs. It serves as a building block in organic reactions where the methoxy and methyl groups aid in directing substitution patterns during drug development. Also employed in the preparation of agrochemicals and specialty heterocyclic compounds due to its stable pyridine ring and reactive sites. Its derivatives are explored in research for potential bioactive molecules and catalysts in asymmetric synthesis.

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