5-Methoxypicolinaldehyde

95%

Reagent Code: #206460
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CAS Number 22187-96-8

science Other reagents with same CAS 22187-96-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 137.14 g/mol
Formula C₇H₇NO₂
thermostat Physical Properties
Boiling Point 248.3°C
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its aldehyde functionality allows for easy derivatization, making it valuable in forming imines, oximes, or undergoing reduction to produce corresponding alcohols or amines. Commonly employed in medicinal chemistry for building heterocyclic compounds due to its pyridine core with electron-donating methoxy group, which enhances reactivity and selectivity in coupling reactions. Also utilized in agrochemical research for designing novel pesticides and herbicides. Its structural features support improved solubility and binding affinity in final active compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿440.00
inventory 250mg
10-20 days ฿900.00
inventory 1g
10-20 days ฿2,720.00
inventory 5g
10-20 days ฿11,210.00
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5-Methoxypicolinaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its aldehyde functionality allows for easy derivatization, making it valuable in forming imines, oximes, or undergoing reduction to produce corresponding alcohols or amines. Commonly employed in medicinal chemistry for building heterocyclic compounds due to its pyridine core with electron-donating methoxy group, which enhances reactivity and selectivity in co

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its aldehyde functionality allows for easy derivatization, making it valuable in forming imines, oximes, or undergoing reduction to produce corresponding alcohols or amines. Commonly employed in medicinal chemistry for building heterocyclic compounds due to its pyridine core with electron-donating methoxy group, which enhances reactivity and selectivity in coupling reactions. Also utilized in agrochemical research for designing novel pesticides and herbicides. Its structural features support improved solubility and binding affinity in final active compounds.

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