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Structure of 33233-67-9
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This protected amino acid derivative features a tert-butoxycarbonyl group that stabilizes the amine functionality, enabling straightforward deprotection under mild acidic conditions. The para-substituted benzoic acid moiety provides a rigid aromatic handle for conjugation or incorporation into peptide-based systems, offering enhanced solubility and compatibility in synthetic workflows.
4-(((tert-Butoxycarbonyl)amino)methyl)benzoic acid serves as a versatile building block for the synthesis of biologically relevant scaffolds, enabling efficient introduction of both carboxylic acid and protected amine functionalities. Its tert-butyl carbamate group offers excellent bench stability and compatibility with standard peptide coupling protocols, while the aromatic methylamine linker facilitates selective transformations. The molecule functions effectively in multi-step syntheses requiring orthogonal protection strategies.
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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: