4-Methoxypicolinaldehyde

98%

Reagent Code: #206438
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CAS Number 16744-81-3

science Other reagents with same CAS 16744-81-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 137.14 g/mol
Formula C₇H₇NO₂
badge Registry Numbers
MDL Number MFCD08234865
thermostat Physical Properties
Boiling Point 238.6°C
inventory_2 Storage & Handling
Storage -20°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 and methoxy functional groups allow for selective reactions, making it valuable in constructing complex heterocyclic compounds. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modify molecular polarity and binding affinity. Also utilized in agrochemical research for designing novel active ingredients with improved stability and efficacy.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,320.00
inventory 5g
10-20 days ฿6,950.00
inventory 10g
10-20 days ฿12,280.00
inventory 25g
10-20 days ฿30,000.00
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4-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 and methoxy functional groups allow for selective reactions, making it valuable in constructing complex heterocyclic compounds. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modify molecular polarity and binding affinity. Also utilized in agrochemical research for designing novel act
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its aldehyde and methoxy functional groups allow for selective reactions, making it valuable in constructing complex heterocyclic compounds. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modify molecular polarity and binding affinity. Also utilized in agrochemical research for designing novel active ingredients with improved stability and efficacy.
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