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Structure of 89466-18-2
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6-Bromo-2-methoxypyridin-3-amine features a pyridine core bearing bromine at the 6-position and a methoxy group at the 2-position, creating a uniquely activated heterocyclic scaffold. This configuration enables direct coupling reactions in late-stage functionalization. The amine functionality at the 3-position serves as a key handle for C–N bond formation. The molecule exhibits enhanced solubility in polar organic solvents and stability under standard bench conditions, facilitating use in synthetic workflows requiring reliable reactivity and ease of handling.
6-Bromo-2-methoxypyridin-3-amine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its well-defined bromine handle and compatible methoxy and amino substituents. The molecule exhibits excellent bench stability and facilitates efficient functionalization in late-stage diversification of heterocyclic scaffolds. Its orthogonal reactivity profile supports selective transformations in complex synthesis 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: