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Structure of 13445-16-4
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3-Bromo-2,6-dimethoxypyridine features a pyridine core functionalized with bromo and two methoxy groups at strategic positions, enabling selective cross-coupling reactions. The electron-rich aromatic ring facilitates palladium-catalyzed transformations, while the sterically protected ortho-methoxy substituents enhance stability and regiocontrol in synthetic sequences. This compound serves as a key intermediate in pharmaceutical and agrochemical synthesis.
3-Bromo-2,6-dimethoxypyridine serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its stable bromo group and electron-rich pyridine core. The ortho-dimethoxy substitution enhances regioselectivity in C–H functionalization and facilitates downstream derivatization for pharmaceutical intermediates. Its bench-stable nature and compatibility with standard reaction conditions make it ideal for iterative 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: