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Structure of 14704-64-4
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4-Amino-6-chloropyridazin-3(2H)-one features a fused heterocyclic core with complementary electron-rich and electrophilic sites, enabling direct functionalization in medicinal chemistry. The amino group facilitates coupling reactions, while the chloro substituent serves as a regioselective handle for nucleophilic substitution under mild conditions. This scaffold exhibits favorable solubility and stability under standard bench protocols, making it a practical building block for targeted library synthesis.
4-Amino-6-chloropyridazin-3(2H)-one serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted pyridazinones via nucleophilic displacement or cross-coupling. The chloro group facilitates direct functionalization under mild conditions, while the amino and carbonyl functionalities provide orthogonal handles for further derivatization. Bench-stable and readily purified by recrystallization, it functions effectively in standard synthetic workflows for heterocyclic scaffold 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-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: