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Structure of 943654-33-9
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2-(6-Chloro-1H-indol-1-yl)acetic acid features a chlorinated indole core linked to a carboxylic acid side chain, enabling direct conjugation in bioactive molecule synthesis. The electron-deficient aromatic system enhances reactivity in coupling reactions, while the pendant acid group facilitates derivatization under standard conditions. This scaffold supports targeted drug discovery efforts involving indole-based pharmacophores.
2-(6-Chloro-1H-indol-1-yl)acetic acid serves as a key building block for indole-based pharmaceutical intermediates, enabling efficient conjugation via amide and ester formation. Its bench-stable nature and compatibility with standard coupling reactions facilitate straightforward derivatization. The molecule functions as a versatile scaffold in the synthesis of bioactive heterocycles and supports orthogonal functional group manipulation 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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: