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Structure of 6231-18-1
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2,6-Dimethoxypyridine serves as a versatile heterocyclic scaffold featuring two methoxy groups at electron-rich positions. This configuration enhances nucleophilicity at the pyridine ring while improving solubility in organic media. The molecule exhibits bench-stable behavior under standard conditions and functions effectively in coupling reactions, transition metal catalysis, and synthetic route development.
2,6-Dimethoxypyridine serves as a versatile building block in synthetic organic chemistry, offering enhanced nucleophilicity at the pyridine nitrogen due to the electron-donating methoxy groups. It functions effectively as a directing group in transition-metal-catalyzed C–H functionalization and facilitates regioselective substitution reactions. The compound exhibits excellent bench stability and ease of purification, making it well-suited for iterative synthesis workflows and the construction of complex heterocyclic scaffolds relevant to medicinal chemistry and agrochemical development.
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1760
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H227-H302-H315-H318-H335
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Precautionary Statements : P210-P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P370+P378-P405-P501
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Lot numbers can be found on the outside label of a product: