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Structure of 5257-24-9
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3-Methylindole-2-carboxaldehyde features a fused indole core with a methyl group at the 3-position and an aldehyde functional group at the 2-position, enabling direct integration into heterocyclic synthesis. The electron-rich indole system pairs with the reactive aldehyde for efficient coupling reactions. This compound serves as a key building block in medicinal chemistry and materials science.
3-Methylindole-2-carboxaldehyde serves as a versatile building block in medicinal chemistry, enabling efficient access to indole-based scaffolds through standard aldehyde functional group transformations. Its bench-stable nature and compatibility with amine coupling, reductive amination, and nucleophilic addition reactions facilitate straightforward synthesis of bioactive heterocycles. The molecule functions effectively in multistep sequences where orthogonality and predictable reactivity are essential for target-oriented synthesis.
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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-H412
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Precautionary Statements : P264-P270-P273-P330-P501
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Lot numbers can be found on the outside label of a product: