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*For research and further manufacturing use only, not for direct human use.
Structure of 21209-51-8
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Z-Ser-OBzl features a protected serine side chain with orthogonal functionality, enabling selective coupling in peptide synthesis. The benzyl ester group ensures stability during reaction sequences while allowing clean deprotection under standard conditions. This derivative facilitates efficient access to complex peptide architectures without compromising stereochemical integrity.
Z-Ser-OBzl serves as a key chiral building block in peptide synthesis, offering stable protection of both amine and hydroxyl functionalities. The benzyloxycarbonyl (Z) group provides robust amine protection compatible with standard deprotection protocols, while the benzyl (OBzl) ester protects the serine side chain without interfering with coupling reactions. Its bench-stable nature and compatibility with diverse coupling reagents facilitate efficient assembly of complex peptide sequences and glycopeptide scaffolds.
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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: