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Structure of 93247-78-0
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Methyl 1H-indole-7-carboxylate features a strategically positioned ester group at the C7 position of the indole scaffold, enabling selective functionalization in synthetic routes. This bench-stable derivative offers enhanced solubility and reactivity compared to the parent carboxylic acid, facilitating its use in transition-metal-catalyzed couplings and bioconjugation strategies.
Methyl 1H-indole-7-carboxylate serves as a versatile building block for indole-based heterocycles, enabling direct functionalization at the C7 position. Its ester group facilitates subsequent transformations including hydrolysis, reduction, and cross-coupling reactions. The molecule exhibits good bench stability and is compatible with a range of standard synthetic conditions, making it well-suited for medicinal chemistry campaigns and API intermediate 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: