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Structure of 35677-88-4
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N-Carbobenzoxy-L-homoserine features a protected amino group and a reactive hydroxyl side chain, enabling direct incorporation into peptide synthesis workflows. The benzyloxycarbonyl (Cbz) moiety ensures stability during handling and reaction sequencing. This derivative serves as a key precursor for homoserine-containing peptides in medicinal chemistry and bioconjugation applications.
N-Carbobenzoxy-L-homoserine serves as a key building block in peptide synthesis and heterocyclic chemistry, offering a stable, bench-ready precursor for L-homoserine-derived scaffolds. Its carboxybenzoyl (Cbz) group provides orthogonal protection for the amine, enabling selective deprotection and coupling under standard conditions. The molecule facilitates efficient construction of β-hydroxy amino acid motifs and supports diverse functionalization, including esterification and cyclization reactions, with high reproducibility in synthetic 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-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: