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Structure of 1849-53-2
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3-Methoxypicolinaldehyde features a pyridine ring with strategically positioned aldehyde and methoxy groups, enabling direct incorporation into bioactive scaffolds. The electron-withdrawing aldehyde enhances reactivity in nucleophilic addition reactions, while the para-methoxy substituent improves solubility and stability under standard conditions. This compound serves as a key building block for pharmaceutical intermediates and functional materials.
3-Methoxypicolinaldehyde serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridine-based heterocycles. Its aldehyde functionality facilitates nucleophilic additions and condensation reactions, while the methoxy group enhances solubility and modulates electronic properties. The compound exhibits excellent bench stability and compatibility with standard purification methods, making it well-suited for multi-step synthesis and scale-up applications.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: