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Structure of 53940-90-2
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N-[(1,1-Dimethylethoxy)carbonyl]-2-methyl-L-valine features a stable tert-butoxycarbonyl (Boc) protecting group and a branched aliphatic side chain, enabling efficient incorporation into peptide synthesis. This bench-stable amino acid derivative facilitates sequential coupling under standard conditions while minimizing racemization.
N-[(1,1-Dimethylethoxy)carbonyl]-2-methyl-L-valine serves as a protected amino acid building block for peptide synthesis, offering enhanced stability and ease of purification. The tert-butoxycarbonyl (Boc) group provides reliable orthogonal protection under acidic conditions, while the branched aliphatic side chain supports steric control in sequence assembly. Functions effectively in standard coupling protocols and facilitates efficient deprotection, making it a practical choice for both manual and automated synthesis 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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: