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Structure of 1893125-36-4
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6-Chloro-2-methyl-2H-indazol-5-amine features a chlorinated indazole core with a methyl group at the 2-position and a primary amine at the 5-position. This electron-deficient scaffold enables direct coupling in cross-coupling reactions, serving as a key building block for bioactive heterocycles in medicinal chemistry and agrochemical development.
6-Chloro-2-methyl-2H-indazol-5-amine serves as a versatile building block for medicinal chemistry and agrochemical synthesis, enabling efficient construction of indazole-based scaffolds. The chloro group facilitates palladium-catalyzed cross-coupling reactions, while the primary amine supports derivatization via acylation, alkylation, or reductive amination. Bench-stable and readily purified by chromatography, it functions reliably in standard synthetic workflows requiring functional group tolerance and predictable reactivity.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: