4-(Benzyloxy)picolinaldehyde

98%

Reagent Code: #150933
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CAS Number 63071-14-7

science Other reagents with same CAS 63071-14-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.23 g/mol
Formula C₁₃H₁₁NO₂
badge Registry Numbers
MDL Number MFCD18256122
thermostat Physical Properties
Melting Point 89.5 °C
inventory_2 Storage & Handling
Density 1.191±0.06 g/cm3(Predicted)
Storage 2-8°C, inert atmosphere

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active molecules. Its aldehyde and ether functional groups allow for versatile chemical modifications, making it valuable in constructing complex organic frameworks. Commonly employed in cross-coupling reactions, condensations, and reductive amination processes to build nitrogen-containing heterocycles. Also utilized in medicinal chemistry for the preparation of pyridine-based drug candidates targeting cancer, inflammation, and central nervous system disorders.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,800.00
inventory 250mg
10-20 days ฿21,500.00
inventory 1g
10-20 days ฿36,200.00

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4-(Benzyloxy)picolinaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active molecules. Its aldehyde and ether functional groups allow for versatile chemical modifications, making it valuable in constructing complex organic frameworks. Commonly employed in cross-coupling reactions, condensations, and reductive amination processes to build nitrogen-containing heterocycles. Also utilized in medicinal chemistry for the preparation of pyri

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active molecules. Its aldehyde and ether functional groups allow for versatile chemical modifications, making it valuable in constructing complex organic frameworks. Commonly employed in cross-coupling reactions, condensations, and reductive amination processes to build nitrogen-containing heterocycles. Also utilized in medicinal chemistry for the preparation of pyridine-based drug candidates targeting cancer, inflammation, and central nervous system disorders.

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