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Structure of 104060-23-3
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N-Boc-2-(4-Aminophenyl)ethanol features a protected primary amine tethered to a phenethyl scaffold, enabling direct incorporation into peptide and small-molecule libraries. The Boc group ensures stability during synthetic manipulations while allowing selective deprotection under mild acidic conditions. This compound serves as a key intermediate for bioactive molecule synthesis, particularly in kinase inhibitor development and functionalized arylamine architectures.
N-Boc-2-(4-Aminophenyl)ethanol serves as a versatile building block for the synthesis of arylalkylamine-containing scaffolds. The Boc-protected amine enables orthogonal functional group manipulation, while the pendant phenolic hydroxyl supports direct derivatization or coupling reactions. This compound facilitates efficient access to bioactive heterocycles and pharmaceutical intermediates through standard amine deprotection and cross-coupling protocols.
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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: