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Structure of 1044872-40-3
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Methyl 2-amino-4,6-dichloronicotinate features a strategically positioned amino group flanked by two chlorine atoms on the pyridine ring, enhancing its reactivity in cross-coupling and cyclization reactions. This bench-stable derivative integrates readily into complex heterocyclic architectures, offering high functional group tolerance and predictable regiochemistry under standard conditions.
Methyl 2-amino-4,6-dichloronicotinate serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted pyridine scaffolds. Its amino and ester functionalities offer orthogonal reactivity for downstream transformations, including nucleophilic substitutions, coupling reactions, and heterocycle elaboration. The molecule exhibits good bench stability and facilitates straightforward purification, making it well-suited for use in multi-step synthesis and API development workflows.
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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: