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Structure of 16176-74-2
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2-(1H-Indol-4-yl)acetic acid features a planar indole core with a pendant carboxylic acid group, enabling direct conjugation in bioactive molecule synthesis. This configuration supports hydrogen bonding and π-stacking interactions, enhancing binding affinity in receptor-targeted applications. The molecule exhibits robust stability under standard bench conditions and integrates readily into peptide and small-molecule frameworks.
2-(1H-Indol-4-yl)acetic acid serves as a versatile building block for the synthesis of indole-containing bioactive molecules, enabling efficient conjugation via amide and ester linkages. Its bench-stable nature and compatibility with standard peptide coupling protocols facilitate straightforward derivatization. Functions as a key intermediate in the construction of heterocyclic scaffolds and prodrugs relevant to 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: