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Structure of 938-97-6
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2-Amino-2-(4-hydroxyphenyl)acetic acid features a phenolic hydroxyl group flanked by an amino-substituted acetic acid backbone, enabling integration into bioconjugation workflows and peptide synthesis. This bench-stable scaffold offers enhanced solubility in aqueous media and serves as a key building block for functionalized molecular probes and pharmaceutical intermediates.
2-Amino-2-(4-hydroxyphenyl)acetic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of phenolic β-amino acids and related scaffolds. Its dual functionality—amine and phenolic hydroxyl—supports diverse derivatization pathways, including amidation, esterification, and metal-catalyzed coupling reactions. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis campaigns and API intermediate development.
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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: