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Structure of 443956-21-6
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Methyl 6-amino-3,5-dibromopicolinate features a brominated pyridine core with complementary amino and ester functionalities. This electron-deficient heterocycle enables direct coupling in cross-coupling reactions and serves as a key intermediate in the synthesis of bioactive molecules. The molecule exhibits enhanced solubility in polar organic solvents and stability under standard bench conditions, facilitating its use in medicinal chemistry workflows.
Methyl 6-amino-3,5-dibromopicolinate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to brominated pyridine scaffolds. The amino and methyl ester functionalities provide orthogonal handles for sequential functionalization, while the dibromo substitution pattern supports palladium-catalyzed cross-coupling reactions. Its bench-stable nature and compatibility with standard purification methods make it well-suited for medicinal chemistry and process development workflows.
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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: