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Structure of 6082-66-2
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3,4,6-Trichloropyridazine is a highly functionalized heterocycle featuring three chlorine substituents at key positions on the pyridazine ring. This electron-deficient scaffold enables direct coupling in cross-coupling reactions and serves as a robust building block for pharmaceutical intermediates. The molecule exhibits enhanced stability under standard conditions, facilitating straightforward incorporation into complex molecular architectures.
3,4,6-Trichloropyridazine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of complex heterocyclic scaffolds. Its three chlorine substituents provide orthogonal reactivity for sequential cross-coupling or nucleophilic substitution reactions, facilitating the installation of diverse aryl, heteroaryl, and amine functionalities. The molecule exhibits good bench stability and is compatible with standard reaction conditions, making it well-suited for iterative synthetic strategies in API development.
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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: