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Structure of 10590-73-5
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3-Methyl-1H-indole-2-carboxylic acid features a fused indolic core with a methyl group at the 3-position and a carboxylic acid at C2, enabling direct integration into bioactive molecule scaffolds. This electron-deficient heterocycle serves as a key building block in medicinal chemistry, particularly for targeting receptor-ligand interactions in CNS and oncology applications.
3-Methyl-1H-indole-2-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling efficient access to indole-based scaffolds through standard amide coupling and decarboxylation protocols. Its carboxylic acid functionality exhibits excellent compatibility with diverse reaction conditions, while the methyl-substituted indole core provides enhanced stability and favorable solubility for bench-scale synthesis. Functions effectively in solid-phase and solution-phase workflows, facilitating rapid diversification of bioactive heterocycles.
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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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: