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Structure of 45170-31-8
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This chiral building block features a protected amino acid scaffold with a tert-butoxycarbonyl (Boc) group and a methylamino side chain, enabling straightforward deprotection and functionalization. The (2S)-configuration ensures stereochemical fidelity in peptide synthesis, while the branched isovaleryl side chain imparts steric stability and solubility under standard conditions.
(2S)-2-[[(tert-Butoxy)carbonyl](methyl)amino]-3-methylbutanoic acid serves as a versatile chiral building block for peptide synthesis and medicinal chemistry campaigns. Its tert-butyl ester functionality enables orthogonal protection, while the methyl-substituted β-amino acid scaffold facilitates efficient coupling reactions and structural diversity in macrocyclic and peptidomimetic architectures. The compound exhibits excellent bench stability and simplifies purification through standard acid-labile deprotection protocols.
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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: