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Structure of 17325-39-2
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2,6-Dimethoxypyridin-4-amine features a pyridine core functionalized with two methoxy groups and a primary amine at the 4-position. This electron-rich scaffold offers enhanced solubility and stability under standard conditions, enabling efficient incorporation into medicinal chemistry libraries. The para-amino group facilitates direct coupling reactions for building complex heterocyclic architectures.
2,6-Dimethoxypyridin-4-amine serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridine-based scaffolds through nucleophilic substitution and transition-metal-catalyzed coupling reactions. Its two methoxy groups enhance solubility and modulate electronic properties, while the primary amine facilitates derivatization. The compound exhibits bench stability and compatibility with common protecting group strategies, making it well-suited for iterative synthesis workflows in API development.
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GHS Pictogram :
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GHS No : GHS06,GHS09
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H300-H315-H319-H335-H411
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Precautionary Statements : P261-P264-P330
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Lot numbers can be found on the outside label of a product: