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Structure of 6274-82-4
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2,6-Dimethoxyisonicotinic acid features a para-substituted pyridine core with two methoxy groups at the 2- and 6-positions, enhancing solubility and modulating electronic properties. This bench-stable derivative serves as a key building block in medicinal chemistry, particularly for coupling reactions in drug discovery workflows.
2,6-Dimethoxyisonicotinic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of heterocyclic scaffolds and bioactive molecules through established coupling reactions. Its ortho-dimethoxy substitution pattern enhances solubility and provides predictable reactivity in amide formation and Suzuki couplings, while maintaining bench stability and ease of purification.
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Lot numbers can be found on the outside label of a product: