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Structure of 7197-01-5
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6-Chloro-3-methyl[1,2,4]triazolo[4,3-b]pyridazine features a fused triazolopyridazine core with strategic chlorine and methyl substituents, enabling direct integration into bioactive molecule scaffolds. The electron-deficient heterocycle facilitates coupling reactions under mild conditions, while the chloro group serves as a versatile handle for nucleophilic substitution. This compound exhibits bench-stable handling and compatibility with diverse synthetic transformations.
6-Chloro-3-methyl[1,2,4]triazolo[4,3-b]pyridazine serves as a versatile heterocyclic building block in medicinal chemistry, enabling direct functionalization at the C6 chloride site via palladium-catalyzed cross-coupling. Its methyl group at C3 provides regiochemical control and enhances metabolic stability. The triazolopyridazine core exhibits excellent bench stability, facilitating straightforward purification and integration into complex scaffolds. This compound functions effectively in standard SNAr and transition-metal-mediated transformations, making it valuable for rapid library synthesis and 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: