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Structure of 42373-30-8
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4-Aminonicotinaldehyde features a pyridine ring bearing both aldehyde and primary amine functionalities at para positions, enabling dual reactivity in synthetic transformations. This electron-rich scaffold integrates readily into bioactive molecule design, offering enhanced solubility and stability under standard bench conditions for medicinal chemistry applications.
4-Aminonicotinaldehyde serves as a versatile building block in medicinal chemistry, enabling the synthesis of pyridine-based heterocycles and bioactive scaffolds. Its ortho-aldehyde and primary amine functionalities offer complementary reactivity for coupling reactions, Ugi-type condensations, and Schiff base formation. The compound exhibits bench stability and facilitates straightforward purification, making it well-suited for iterative library synthesis and process-scale 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-H317-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P272-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: