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Structure of 192315-36-9
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(S)-2-((tert-butoxycarbonyl)amino)-3-(3-chloro-4-hydroxyphenyl)propanoic acid is a chiral building block featuring a protected amine and a phenolic hydroxyl group. This configuration enables selective conjugation in peptide synthesis, while the electron-withdrawing chlorine enhances reactivity in downstream functionalization. The tert-butyl carbamate moiety provides stability under basic conditions and facilitates orthogonal deprotection.
(S)-2-((tert-butoxycarbonyl)amino)-3-(3-chloro-4-hydroxyphenyl)propanoic acid serves as a key chiral building block for the synthesis of bioactive molecules, particularly in the development of β-amino acid derivatives and peptidomimetics. The protected amine and phenolic hydroxyl groups enable orthogonal functionalization, while the tert-butyl carbamate moiety provides excellent bench stability and ease of purification. This compound facilitates efficient coupling reactions and is well-suited for iterative synthetic sequences 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: