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Structure of 28020-37-3
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3-Amino-2,6-dimethoxypyridine features a pyridine core functionalized with amino and methoxy groups at electron-rich positions, enabling robust coupling in cross-coupling reactions. The ortho-methoxy substituents enhance solubility and stabilize reactive intermediates under standard conditions. This compound serves as a key building block for bioactive heterocycles in medicinal chemistry and agrochemical development.
3-Amino-2,6-dimethoxypyridine serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted pyridine scaffolds via palladium-catalyzed cross-coupling and electrophilic substitution reactions. The amino group facilitates derivatization, while the ortho-dimethoxy arrangement provides enhanced stability and favorable electronic properties for heterocycle construction. Its bench-stable nature and compatibility with diverse 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 : 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: