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Structure of 1227048-73-8
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Methyl 2-amino-6-bromonicotinate features a brominated pyridine core with a strategically positioned amino group and methyl ester, enabling direct incorporation into heterocyclic scaffolds. This bench-stable derivative serves as a key intermediate in the synthesis of bioactive molecules, particularly where halogenated nitrogen-containing rings are required for downstream functionalization or target engagement.
Methyl 2-amino-6-bromonicotinate serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the 2-amino and 6-bromo positions. Its stability under standard bench conditions facilitates straightforward coupling reactions, nucleophilic substitutions, and transition-metal-catalyzed transformations. The molecule functions effectively in constructing heterocyclic scaffolds and drug-like intermediates, offering excellent compatibility with common protecting group strategies and purification 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: