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Structure of 5672-83-3
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N-Benzyloxycarbonyl-L-glutamic acid 1-methyl ester features a protected α-amino group and a selectively functionalized side chain, enabling straightforward incorporation into peptide synthesis workflows. The benzyl ester moiety provides enhanced solubility and stability during coupling steps, while the methyl ester offers controlled deprotection kinetics under standard acidic conditions. This derivative serves as a key building block for synthesizing glutamate-containing peptides with defined stereochemistry.
N-Benzyloxycarbonyl-L-glutamic acid 1-methyl ester serves as a key dipeptide building block in peptide synthesis, offering orthogonal protection of both α-amino and γ-carboxyl functionalities. The benzyloxycarbonyl (Cbz) group ensures stable amino protection under standard coupling conditions, while the methyl ester at the γ-position enables selective deprotection and downstream derivatization. This compound facilitates efficient construction of glutamic acid-containing scaffolds in medicinal chemistry and peptide-based drug discovery, with excellent bench stability and compatibility with common purification methods.
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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: