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Structure of 3392-12-9
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This tert-butoxycarbonyl-protected valine derivative features a reactive dioxopyrrolidinyl leaving group, enabling efficient amide bond formation under mild conditions. The bulky tert-butyl carbamate moiety provides enhanced stability and ease of purification, while the hydrophobic valine side chain supports incorporation into peptide sequences with minimal steric interference.
Boc-L-valine 2,5-dioxopyrrolidin-1-yl ester serves as a robust amino acid coupling agent, enabling efficient amide bond formation in peptide synthesis. The pyrrolidinone ester moiety ensures high reactivity with primary amines under mild conditions, while the tert-butoxycarbonyl (Boc) group provides stable protection of the α-amino function. This compound exhibits excellent bench stability, simplifies purification by precipitation, and is compatible with a broad range of functional groups, making it a reliable building block for fragment assembly and synthetic peptide 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 : H401
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Precautionary Statements : P273-P501
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Lot numbers can be found on the outside label of a product: