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Structure of 779324-37-7
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This pyridine derivative features a strategically positioned aminomethyl group and N-methyl substitution, enabling precise coordination in catalytic systems. The electron-rich aromatic core enhances reactivity in transition-metal-mediated transformations, while the methylated nitrogen improves solubility and metabolic stability. Designed for efficient integration into ligand architectures and bioconjugation workflows under standard conditions.
5-(Aminomethyl)-N-methylpyridin-2-amine serves as a versatile building block in medicinal chemistry, enabling the construction of pyridine-based pharmacophores. Its ortho-amino and methylated nitrogen functionalities provide enhanced solubility and tunable basicity, facilitating downstream derivatization via amide coupling, alkylation, or reductive amination. The molecule exhibits excellent bench stability and compatibility with common protecting group strategies, supporting efficient synthesis of targeted heterocyclic scaffolds.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3259
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: