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Structure of 24985-85-1
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Ethyl 5-hydroxyindole-2-carboxylate features a hydroxylated indole core paired with an ester-functionalized carboxyl group, enabling direct incorporation into diverse heterocyclic architectures. This bench-stable scaffold supports efficient derivatization in medicinal chemistry and materials synthesis workflows.
Ethyl 5-hydroxyindole-2-carboxylate serves as a versatile building block for indole-based heterocycles, enabling direct functionalization at the C5 position via oxidation or coupling reactions. Its hydroxyl group offers a handle for selective derivatization while maintaining compatibility with standard synthetic protocols. The ester functionality facilitates subsequent transformations, including hydrolysis and amidation, supporting access to diverse pharmacophores. Bench-stable and readily purified by chromatography, it functions effectively in medicinal chemistry campaigns requiring controlled indole scaffold elaboration.
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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: