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Structure of 884004-48-2
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2-Amino-4-chloronicotinaldehyde features a strategically positioned aldehyde group flanked by electron-donating amino and electron-withdrawing chloro substituents, enabling precise tuning of reactivity in heterocyclic synthesis. This bench-stable scaffold integrates readily into complex molecular architectures under standard conditions.
2-Amino-4-chloronicotinaldehyde serves as a versatile building block in medicinal chemistry, enabling the synthesis of heterocyclic scaffolds via condensation and cyclization reactions. Its ortho-amino and aldehyde functionalities offer complementary reactivity for constructing fused rings and bioactive molecules, with demonstrated stability under standard bench conditions and ease of purification.
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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: