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Structure of 24277-38-1
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This tert-butyl-protected glutamate derivative features a sterically hindered tert-butoxycarbonyl group and a methyl substituent at the 5-position, enabling stable incorporation into peptide synthesis workflows. The bulky tert-butyl moiety enhances solubility and minimizes racemization during coupling reactions.
1-(tert-Butyl) 5-methyl (tert-butoxycarbonyl)-L-glutamate serves as a versatile diacid protecting group scaffold in peptide synthesis, enabling selective functionalization at the γ-carboxylate while maintaining stability under standard coupling conditions. The tert-butoxycarbonyl (Boc) group provides orthogonal protection to the α-amino function, facilitating sequential assembly of complex peptides and heterocyclic building blocks. Its bench-stable nature and ease of deprotection with mild acid simplify purification workflows and support scalable applications in medicinal chemistry and API development.
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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
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Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: