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Structure of 120739-62-0
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This pyridylamine derivative features a chlorinated pyridine core paired with a methylated amine side chain, enabling integration into bioactive molecule scaffolds. The electron-deficient pyridine ring enhances electrophilic reactivity, while the N-methyl group improves metabolic stability and membrane permeability. This compound serves as a key building block in medicinal chemistry for targeted drug discovery.
1-(6-Chloropyridin-3-yl)-N-methylmethanamine serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the pyridine C6 position. Its tertiary amine functionality facilitates salt formation and improves solubility, while the chloropyridine moiety supports palladium-catalyzed cross-coupling reactions. The compound exhibits bench stability and compatibility with standard purification protocols, making it suitable for iterative synthesis of heterocyclic scaffolds and API intermediates.
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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#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: