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Structure of 3414-19-5
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5-Hydroxy-1H-indole-3-carbaldehyde features a strategically positioned aldehyde group flanked by a hydroxyl and indole scaffold, enabling direct integration into bioactive molecule synthesis. This electron-rich heterocycle exhibits enhanced solubility in polar solvents and stability under standard bench conditions, facilitating its use in medicinal chemistry campaigns targeting serotonin receptor modulators and fluorescent probes.
5-Hydroxy-1H-indole-3-carbaldehyde serves as a versatile building block for heterocyclic synthesis, enabling efficient access to indole-based scaffolds through standard functional group transformations. The aldehyde functionality facilitates reductive amination, condensation, and coupling reactions, while the phenolic hydroxyl group supports derivatization or protection strategies. Its bench-stable nature and compatibility with common reaction conditions make it suitable for medicinal chemistry and process development 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: