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Structure of 22279-89-6
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2,5-Dimethylpyridin-4-amine features a pyridine core with methyl groups at positions 2 and 5, enhancing electron density at the para-amino site. This bench-stable scaffold integrates readily into transition metal-catalyzed coupling reactions, serving as a robust ligand in palladium-mediated transformations. The sterically hindered dimethyl substitution improves stability under oxidative conditions while maintaining nucleophilicity for C–N bond formation.
2,5-Dimethylpyridin-4-amine serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive heterocycles through standard coupling and functionalization reactions. Its pyridine core exhibits favorable electronic properties and bench stability, while the ortho-methyl groups enhance metabolic resistance. The primary amine facilitates conjugation in Suzuki-Miyaura and Buchwald-Hartwig protocols, offering efficient access to complex scaffolds for drug discovery.
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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: