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Structure of 18450-26-5
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Methyl 3-formyl-1H-indole-2-carboxylate features a reactive aldehyde group flanked by electron-rich indole and ester functionalities, enabling direct coupling in cross-coupling and condensation reactions. This bench-stable, moisture-tolerant scaffold integrates readily into complex heterocyclic architectures, streamlining access to biologically relevant indole derivatives.
Methyl 3-formyl-1H-indole-2-carboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted indoles via formyl group transformations. Its dual functionality—aldehyde and ester—supports diverse downstream modifications including reductive amination, condensation reactions, and transition-metal-catalyzed couplings. The molecule exhibits good bench stability and facilitates straightforward purification, making it well-suited for medicinal chemistry campaigns and heterocycle synthesis.
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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: