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Structure of 6692-89-3
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This protected amino acid derivative features a benzylcarbamate (Cbz) group at the N-terminus and a ureido functionality at the C-terminal end, enabling selective incorporation into peptide sequences. The benzyloxy carbonyl moiety ensures stable protection under standard conditions, while the para-ureido side chain offers enhanced solubility and reactivity in synthetic peptide assembly workflows.
Serves as a versatile building block for peptide synthesis and heterocyclic scaffold construction. The (S)-configured amino acid features a benzyloxycarbonyl (Z) protecting group for nitrogen, a pendant ureido function enabling hydrogen-bonding interactions in biomolecular recognition, and a carboxylic acid for coupling reactions. Exhibits excellent bench stability, facilitates efficient purification via standard chromatographic methods, and supports orthogonal functionalization in multi-step synthetic sequences.
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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: