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Structure of 54788-30-6
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This amino acid derivative features a brominated hydroxyphenyl moiety integrated at the β-position, enhancing its utility in bioconjugation and peptide-based drug discovery. The pendant phenolic hydroxyl group enables further derivatization, while the α-amino and carboxylic acid functionalities support robust coupling chemistry under standard conditions.
2-Amino-3-(3-bromo-4-hydroxyphenyl)propanoic acid serves as a versatile building block for bioactive heterocycles and peptide-like scaffolds. Its ortho-hydroxyl and bromo substituents enable efficient downstream functionalization via Suzuki-Miyaura coupling, electrophilic substitution, or metal-catalyzed cross-coupling. The molecule exhibits bench stability, tolerates common protecting group manipulations, and facilitates the synthesis of pharmaceutically relevant arylalanine derivatives through standard peptide 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: