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Structure of 79799-26-1
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This tert-butyl ester derivative features a protected amino group flanked by a methyl-substituted aliphatic chain, enabling stable incorporation into peptide synthesis workflows. The Boc moiety ensures orthogonal handling under standard deprotection conditions, facilitating sequential coupling in complex molecular architectures.
4-((tert-Butoxycarbonyl)amino)-2-methylbutanoic acid serves as a versatile building block for peptide synthesis and medicinal chemistry applications. The Boc-protected amine enables orthogonal functional group manipulation, while the branched aliphatic side chain provides steric differentiation. This compound exhibits excellent bench stability, facilitates straightforward purification via standard chromatographic methods, and participates reliably in standard coupling reactions with minimal epimerization risk.
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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: