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Structure of 1031927-22-6
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6-Chloro-1-methyl-1H-indazol-3-amine features a chlorinated indazoline core with a methylated nitrogen and primary amine functionality. This electron-deficient heterocycle integrates readily into medicinal chemistry scaffolds, offering enhanced metabolic stability and tunable polarity for target engagement in kinase inhibition and CNS drug discovery.
6-Chloro-1-methyl-1H-indazol-3-amine serves as a versatile building block for medicinal chemistry and heterocyclic synthesis, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. The chloro group at the 6-position offers high reactivity in Suzuki, Negishi, and Buchwald–Hartwig couplings, while the 3-amino and 1-methyl substituents provide orthogonal handles for further derivatization. Bench-stable and readily purified by chromatography or recrystallization, it functions reliably in API scaffold development and fragment-based drug discovery workflows.
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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-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: