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Structure of 103986-22-7
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This indole-acetic acid derivative features a methoxy-substituted indole core linked to a carboxylic acid side chain. The electron-donating methoxy group enhances solubility and modulates electronic properties, enabling integration into bioactive scaffolds. Bench-stable and moisture-tolerant, it serves as a key intermediate in the synthesis of serotonin analogs and pharmaceutical candidates targeting neurological pathways.
2-(6-Methoxy-1H-indol-3-yl)acetic acid serves as a versatile building block for indole-based pharmaceutical intermediates, enabling efficient conjugation via amide and ester formation. Its methoxy-substituted indole core offers enhanced metabolic stability and tunable solubility, while the carboxylic acid functionality facilitates straightforward derivatization. The compound exhibits excellent bench stability and is readily purified by recrystallization or chromatography, supporting scalable synthesis in medicinal chemistry campaigns.
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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: