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Structure of 885519-19-7
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Methyl 4-chloro-1H-indazole-6-carboxylate is a bench-stable heterocyclic ester featuring a chlorinated indazole core. This electron-deficient scaffold integrates readily into medicinal chemistry campaigns, serving as a key intermediate for C–H functionalization and Suzuki-Miyaura coupling reactions. The methyl ester group enables straightforward derivatization under mild conditions.
Methyl 4-chloro-1H-indazole-6-carboxylate serves as a versatile building block for the synthesis of indazole-based pharmaceuticals and agrochemicals. The chloro group at the 4-position enables palladium-catalyzed cross-coupling reactions, while the ester functionality supports selective reduction or hydrolysis. Its bench-stable nature and compatibility with diverse reaction conditions facilitate efficient access to functionalized indazole scaffolds in medicinal chemistry workflows.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: