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Structure of 40047-23-2
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6-Hydroxyindole-2-carboxylic acid features a hydroxyl group at the C6 position and a carboxylic acid at C2, enabling direct conjugation or derivatization in bioconjugate chemistry. The molecule integrates readily into peptide scaffolds and offers enhanced solubility compared to non-hydroxylated analogs.
6-Hydroxyindole-2-carboxylic acid serves as a versatile building block for indole-based pharmaceuticals and natural product syntheses. The ortho-hydroxyl and carboxylic acid groups enable direct functionalization, metal coordination, or derivatization via esterification, amidation, or Suzuki coupling. Its stability under standard bench conditions and compatibility with common protecting group strategies facilitate efficient access to complex heterocyclic scaffolds 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 : H319
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Precautionary Statements : P264-P280-P305+P351+P338-P337+P313
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Lot numbers can be found on the outside label of a product: