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Structure of 58584-61-5
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2-Amino-6-chloronicotinaldehyde features a strategically positioned amino group and chloro substituent on the nicotinaldehyde scaffold, enabling selective reactivity in heterocyclic synthesis. This electron-deficient aldehyde integrates readily into advanced intermediates for pharmaceutical development, offering enhanced stability under standard bench conditions.
2-Amino-6-chloronicotinaldehyde serves as a versatile building block in medicinal chemistry, enabling the synthesis of heterocyclic scaffolds via condensation and cyclization reactions. Its dual functionality—amine and aldehyde groups—supports diverse transformations, including imine formation and Ugi-type multicomponent reactions. The chlorine substituent enhances electrophilic reactivity and facilitates further functionalization. Bench-stable and amenable to standard purification protocols, it functions reliably in scale-up processes and combinatorial library synthesis.
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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: