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Structure of 34298-84-5
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This indole derivative features a carboxylic acid group at the 2-position, enabling direct conjugation or derivatization. The indolyl moiety imparts strong π-electron density and planar rigidity, enhancing binding affinity in bioactive molecule design. Stable under standard bench conditions, it serves as a key scaffold for pharmaceutical intermediates and chemical biology probes.
2-(1H-Indol-5-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 carboxylic acid functionality offers high reactivity in standard coupling protocols, while the indole moiety provides a stable, aromatic scaffold compatible with diverse functional group transformations. Bench-stable and readily purified by recrystallization, it functions reliably in medicinal chemistry campaigns targeting CNS-active compounds and peptide conjugates.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: