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Structure of 96551-22-3
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1-Boc-3-Hydroxymethylindole features a protected indole scaffold with a hydroxymethyl side chain, enabling selective functionalization in complex molecule synthesis. The Boc group ensures stability during handling and reaction sequences, while the pendant hydroxyl offers direct access to ether or ester derivatives. This reagent integrates cleanly into multistep pathways requiring controlled indole modification under standard conditions.
1-Boc-3-Hydroxymethylindole serves as a versatile building block for indole-based medicinal chemistry, enabling efficient access to functionalized scaffolds. The Boc group provides excellent stability and orthogonal deprotection under mild acidic conditions, while the hydroxymethyl functionality facilitates downstream transformations such as oxidation to aldehyde, ether formation, or coupling reactions. Its compatibility with standard peptide and heterocyclic synthesis protocols makes it a practical choice for iterative library construction in R&D 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: