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Structure of 23084-36-8
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5-Methoxy-1H-indole-3-carbonitrile features a sterically accessible indole core functionalized with a methoxy group at the 5-position and a nitrile moiety at C3. This electron-deficient scaffold integrates readily into heterocyclic architectures, enabling efficient coupling in transition-metal-catalyzed transformations. The compound exhibits bench-stable handling and enhanced solubility in polar organic solvents, streamlining its use in synthetic medicinal chemistry campaigns.
5-Methoxy-1H-indole-3-carbonitrile serves as a versatile building block for heterocyclic synthesis, enabling efficient access to indole-based scaffolds through standard functional group transformations. Its nitrile group facilitates nucleophilic additions and cyclizations, while the methoxy substituent enhances solubility and modulates electronic properties. Bench-stable and readily purified, it functions effectively in coupling reactions and transition-metal-catalyzed processes common to medicinal chemistry 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
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: