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Structure of 55934-00-4
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3,4-Dichloropyridine serves as a pivotal heterocyclic scaffold in medicinal chemistry and agrochemical synthesis. The ortho-dichloro substitution pattern imparts enhanced electrophilicity at the ring carbon positions, facilitating nucleophilic aromatic substitution reactions. This compound exhibits robust stability under standard conditions and integrates readily into complex molecular architectures via coupling processes.
3,4-Dichloropyridine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient functionalization at the 3- and 4-positions via palladium-catalyzed cross-coupling reactions. Its dual chloro substituents offer orthogonal reactivity for sequential transformations, while the pyridine core provides excellent stability and compatibility with diverse reaction conditions. This compound functions effectively in C–H activation, nucleophilic substitution, and heterocycle elaboration workflows, facilitating rapid access to complex scaffolds used in drug discovery and materials science.
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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: