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Structure of 71420-95-6
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This boronic acid derivative features a para-substituted aryl group flanked by a carboxylic acid and a tert-butoxycarbonyl-protected amine, enabling direct incorporation into peptide-coupling workflows. The Boc moiety provides stability during synthesis and can be selectively removed under mild acidic conditions, streamlining access to functionalized intermediates for medicinal chemistry applications.
2-(3-(((tert-Butoxycarbonyl)amino)methyl)phenyl)acetic acid serves as a versatile building block for the synthesis of biologically relevant scaffolds, enabling efficient access to phenylalanine-derived motifs and heterocyclic systems. The protected amine group offers excellent stability and orthogonal deprotection compatibility, while the pendant carboxylic acid facilitates coupling reactions under standard conditions. Its well-defined reactivity profile supports reliable functionalization in medicinal chemistry campaigns 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: