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Structure of 175461-34-4
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2,6-Dichloro-N,N-dimethylpyridin-4-amine features a pyridine core bearing two ortho-chloro substituents and a dimethylamino group at the 4-position, delivering enhanced electron-withdrawing character. This configuration enables efficient coupling in cross-coupling reactions, particularly in Pd-catalyzed processes where steric and electronic balance improves reaction kinetics. The molecule exhibits excellent bench stability and handles well under standard conditions.
2,6-Dichloro-N,N-dimethylpyridin-4-amine serves as a versatile building block in medicinal chemistry, enabling efficient construction of heterocyclic scaffolds via palladium-catalyzed cross-coupling reactions. The dichloro substitution pattern provides orthogonal reactivity for sequential functionalization, while the dimethylamino group enhances solubility and facilitates purification. Bench-stable and compatible with standard synthetic workflows, it functions reliably in the synthesis of bioactive molecules and complex intermediates.
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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: