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Structure of 17285-36-8
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5,6-Dichloropyridazin-3(2H)-one serves as a versatile heterocyclic scaffold in medicinal chemistry, featuring two chlorine substituents that enhance electrophilicity and facilitate downstream functionalization. This bench-stable, moisture-tolerant compound integrates readily into bioactive molecule design, offering high reactivity in nucleophilic substitution processes under standard conditions.
5,6-Dichloropyridazin-3(2H)-one serves as a versatile building block in medicinal chemistry, enabling efficient construction of nitrogen-containing heterocycles. Its dichloro substitution pattern facilitates selective nucleophilic aromatic substitution, allowing straightforward functionalization at either ring position. The pyridazinone core exhibits excellent bench stability and compatibility with common reaction conditions, simplifying purification and integration into multi-step synthetic sequences. This compound functions as a key intermediate for bioactive scaffolds found in agrochemicals and pharmaceutical development.
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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: