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Structure of 14161-11-6
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3,4,5-Trichloropyridazine is a highly reactive heterocyclic scaffold featuring three chlorine substituents positioned at the 3-, 4-, and 5-positions of the pyridazine ring. This arrangement imparts strong electron-withdrawing character and facilitates selective nucleophilic substitution under mild conditions. The molecule serves as a key intermediate in the synthesis of advanced agrochemicals and pharmaceutical candidates, where its halogenated framework enables efficient coupling reactions. Its bench-stable nature supports reliable handling in multi-step synthetic sequences.
3,4,5-Trichloropyridazine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of nitrogen-containing heterocycles via nucleophilic substitution. Its three chlorine substituents provide orthogonal reactivity for sequential functionalization, facilitating the installation of diverse aryl, alkyl, and amino groups under mild conditions. The compound exhibits excellent bench stability and compatibility with standard coupling protocols, making it ideal for modular scaffold development in high-throughput screening campaigns.
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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: