4-Methoxy-2,3,5-trimethylpyridine

95%

Reagent Code: #210171
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CAS Number 109371-19-9

science Other reagents with same CAS 109371-19-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 151.21 g/mol
Formula C₉H₁₃NO
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MDL Number MFCD12964312
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of vitamin B6 (pyridoxine) and related compounds. It serves as a building block in organic reactions where substituted pyridines are required, especially in the development of drugs targeting neurological and metabolic disorders. Its methoxy and methyl functional groups enhance reactivity and selectivity in coupling reactions, making it valuable in medicinal chemistry and industrial-scale synthesis. Also employed in the preparation of agrochemicals and specialty chemicals due to its stable aromatic structure and modifiable ring system.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,710.00
inventory 1g
10-20 days ฿6,810.00
inventory 5g
10-20 days ฿34,050.00

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4-Methoxy-2,3,5-trimethylpyridine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of vitamin B6 (pyridoxine) and related compounds. It serves as a building block in organic reactions where substituted pyridines are required, especially in the development of drugs targeting neurological and metabolic disorders. Its methoxy and methyl functional groups enhance reactivity and selectivity in coupling reactions, making it valuable in medicinal chemistry and industrial-scale synthesis. Also employed

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of vitamin B6 (pyridoxine) and related compounds. It serves as a building block in organic reactions where substituted pyridines are required, especially in the development of drugs targeting neurological and metabolic disorders. Its methoxy and methyl functional groups enhance reactivity and selectivity in coupling reactions, making it valuable in medicinal chemistry and industrial-scale synthesis. Also employed in the preparation of agrochemicals and specialty chemicals due to its stable aromatic structure and modifiable ring system.

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