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Structure of 167479-16-5
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1-Methylindole-7-carboxylic acid features a sterically accessible carboxyl group appended to the indole core, enabling direct conjugation in bioconjugation workflows. The methyl substitution enhances metabolic stability and modulates electronic properties, making this scaffold valuable for designing targeted therapeutics and fluorescent probes.
1-Methylindole-7-carboxylic acid serves as a versatile building block for indole-based pharmaceutical scaffolds, enabling efficient derivatization at the carboxylic acid group. Its bench-stable nature and compatibility with standard coupling protocols facilitate straightforward amide, ester, and acyl chloride formation. The molecule functions effectively in peptide synthesis and heterocyclic extensions, offering predictable reactivity and excellent functional group tolerance in medicinal chemistry workflows.
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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: