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Structure of 16732-57-3
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Ethyl 5-nitro-1H-indole-2-carboxylate features a nitro-substituted indole core with a strategically positioned ester group, enabling direct functionalization in heterocyclic synthesis. The electron-deficient aromatic system enhances reactivity in cross-coupling and cycloaddition reactions, while the ethyl ester facilitates subsequent hydrolysis or derivatization. This compound serves as a key intermediate in the development of bioactive nitrogen-containing scaffolds.
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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: