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Structure of 210346-16-0
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(S)-2-(((tert-Butoxycarbonyl)amino)methyl)-3-methylbutanoic acid features a chiral α-amino acid backbone with a protected amine and hydrophobic side chain. This bench-stable building block integrates seamlessly into peptide synthesis workflows, enabling efficient access to complex peptidomimetics and bioactive scaffolds under standard conditions.
(S)-2-(((tert-Butoxycarbonyl)amino)methyl)-3-methylbutanoic acid serves as a valuable chiral building block in peptide synthesis, enabling the construction of sterically hindered amino acid motifs. The tert-butyl ester and carbamate groups provide orthogonal protection for carboxylic acid and amine functionalities, facilitating sequential coupling reactions. Its bench-stable nature and compatibility with standard deprotection protocols make it well-suited for multi-step synthetic sequences in medicinal chemistry and API 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: