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Structure of 54781-93-0
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Dimethyl 1H-indole-2,3-dicarboxylate features a rigid indole core with two ester-functionalized positions, enabling direct incorporation into heterocyclic syntheses. The para-substituted diester motif supports transition-metal-catalyzed couplings and serves as a versatile scaffold for medicinal chemistry campaigns. This bench-stable derivative exhibits favorable solubility in common organic solvents and maintains integrity under standard reaction conditions.
Dimethyl 1H-indole-2,3-dicarboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted indole scaffolds. Its dual ester functionality supports selective derivatization and participates reliably in palladium-catalyzed cross-coupling reactions. The molecule exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for iterative synthetic sequences in medicinal chemistry and process development.
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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: