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Structure of 122475-57-4
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2,3-Dimethylpyridin-4-amine features a pyridine core with methyl groups at positions 2 and 3, enhancing electron density at the nitrogen lone pair. This configuration imparts improved solubility and stability in polar solvents, facilitating use in transition metal catalysis and pharmaceutical synthesis. The para-amino substitution enables direct coupling reactions under mild conditions.
2,3-Dimethylpyridin-4-amine serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive heterocycles through palladium-catalyzed cross-coupling and electrophilic substitution reactions. Its pyridine core exhibits favorable solubility and bench stability, while the ortho-methyl groups enhance metabolic resistance and modulate electronic properties. The primary amine functions as a direct handle for derivatization, facilitating rapid access to diverse analogs in lead optimization campaigns.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2671
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Class : 6.1
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Packing Group : Ⅱ
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Hazard Statements : H301-H311-H315-H319-H332-H335
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: