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Structure of 671215-52-4
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2-Methyl-1H-indole-5-carboxaldehyde features a conjugated aldehyde group at the 5-position of a methyl-substituted indole core, enabling direct integration into heterocyclic scaffolds. The electron-rich indole system enhances reactivity in nucleophilic addition and condensation reactions, while the aldehyde moiety offers a handle for diversification via imine formation or reductive amination. This compound serves as a key intermediate in the synthesis of bioactive molecules and functionalized materials.
2-Methyl-1H-indole-5-carboxaldehyde serves as a versatile building block for heterocyclic synthesis, enabling efficient access to indole-based scaffolds through standard coupling and functionalization reactions. The aldehyde group facilitates nucleophilic additions and condensation processes, while the methyl-substituted indole core offers enhanced stability and compatibility with diverse reaction conditions. Its bench-stable nature and predictable reactivity make it ideal for medicinal chemistry campaigns and process development 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 : H302-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P501
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Lot numbers can be found on the outside label of a product: