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Structure of 6127-17-9
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6-Chloro-2-methyl-1H-indole is a bench-stable, electron-deficient indole derivative featuring a chloro group at the 6-position and a methyl substituent at the 2-position. This substitution pattern enhances regioselectivity in electrophilic aromatic substitution reactions and supports efficient incorporation into bioactive heterocycles.
6-Chloro-2-methyl-1H-indole serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the C3 position via palladium-catalyzed cross-coupling reactions. Its electron-deficient indole core enhances reactivity in electrophilic substitutions, while the methyl group provides steric control and metabolic stability. Bench-stable and readily purified by flash chromatography, it functions effectively in the synthesis of kinase inhibitors, CNS-targeted compounds, and other heterocyclic scaffolds requiring halogenated indoles.
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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 : H301
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: