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Structure of 24662-37-1
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1-Methyl-1H-indole-3-carbonitrile features a conjugated indole core with a methyl group at the nitrogen and a nitrile substituent at the 3-position, enabling integration into bioactive molecules. This electron-deficient heterocycle facilitates transition-metal-catalyzed couplings and serves as a key scaffold in medicinal chemistry. The compound exhibits bench-stable handling characteristics and enhanced solubility in organic solvents.
1-Methyl-1H-indole-3-carbonitrile serves as a versatile building block in medicinal chemistry, enabling efficient access to indole-based scaffolds through standard functional group transformations. Its nitrile group facilitates nucleophilic addition and cyclization reactions, while the methylated indole core offers enhanced stability and favorable solubility for downstream synthesis. The compound functions reliably in cross-coupling and heterocycle formation protocols, supporting scalable workflows in API development.
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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-H319
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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: