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Structure of 900800-02-4
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Methyl (S)-2-((tert-butoxycarbonyl)amino)-3-(3-hydroxyphenyl)propanoate features a chiral α-amino acid scaffold with a protected amine and a phenolic hydroxyl group. This bench-stable derivative integrates a para-hydroxyaryl moiety, enabling direct incorporation into peptide sequences or further functionalization. The tert-butyl carbamate group ensures compatibility with standard deprotection protocols in synthetic workflows.
Methyl (S)-2-((tert-butoxycarbonyl)amino)-3-(3-hydroxyphenyl)propanoate serves as a versatile chiral building block for the synthesis of biologically relevant scaffolds. The protected amino group enables selective deprotection and derivatization, while the pendant phenolic hydroxyl and ester functionalities support orthogonal transformations. This compound exhibits excellent bench stability and facilitates efficient purification, making it well-suited for multi-step peptide-like and heterocyclic syntheses 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: