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Structure of 863658-70-2
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This chiral dipeptide derivative features a (2S,3S)-configured backbone with a sterically hindered methyl group and a protected amino terminus. The trimethylsilyl-protected alkoxy carbonyl moiety enables stable handling and selective deprotection during peptide synthesis workflows.
(2S,3S)-3-methyl-2-[2-({[2-(trimethylsilyl)ethoxy]carbonyl}amino)acetamido]pentanoic acid serves as a valuable chiral building block for the synthesis of peptidomimetics and β-lactam antibiotics. Its protected amine and carboxylic acid functionalities enable orthogonal transformations, while the trimethylsilyl ether enhances stability and facilitates purification. The stereochemistry supports predictable reactivity in standard coupling protocols, making it suitable for modular peptide assembly and late-stage functionalization.
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Lot numbers can be found on the outside label of a product: