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Structure of 390427-07-3
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2-(Boc-aminomethyl)phenol features a protected amine tethered to a phenolic backbone, enabling seamless incorporation into peptide and small-molecule syntheses. The Boc group ensures stability during handling and reaction sequences, while the hydroxyl moiety offers a site for derivatization. This scaffold supports modular assembly in medicinal chemistry and combinatorial libraries.
2-(Boc-aminomethyl)phenol serves as a versatile building block for the synthesis of bioactive heterocycles and pharmaceutical intermediates. The Boc-protected amine enables orthogonal functional group manipulation, while the phenolic hydroxyl supports direct derivatization or metal-catalyzed coupling reactions. Its bench-stable nature and compatibility with standard deprotection protocols facilitate efficient multi-step synthesis 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-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: