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*For research and further manufacturing use only, not for direct human use.
Structure of 59279-60-6
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Boc-Glu(OMe)-OMe serves as a protected glutamic acid derivative featuring methyl ester groups at both carboxyl termini and a tert-butoxycarbonyl group on the α-amino function. This configuration enables direct incorporation into peptide synthesis workflows without side-chain protection adjustments, offering enhanced stability and simplified purification under standard conditions.
Boc-Glu(OMe)-OMe serves as a versatile diester building block for the synthesis of glutamic acid-derived peptides and heterocyclic scaffolds. Its orthogonal protection—tert-butoxycarbonyl (Boc) at the α-amino group and methyl esters at both carboxyl termini—enables selective deprotection and sequential coupling in solid-phase and solution-phase syntheses. The compound exhibits excellent bench stability, facilitates straightforward purification, and functions reliably in standard peptide coupling protocols, making it a practical choice for medicinal chemistry and process development 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: