Lot numbers can be found on the outside label of a product:
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*For research and further manufacturing use only, not for direct human use.
Structure of 198544-94-4
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This chiral fluorenonyl-protected amino acid derivative features a sterically hindered side chain and a bench-stable carbamate group, enabling efficient incorporation into peptide synthesis workflows. The diphenyl(p-tolyl)methyl moiety provides robust protection, while the (R)-configuration ensures stereoselective coupling under standard conditions.
(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-6-((diphenyl(p-tolyl)methyl)amino)hexanoic acid serves as a versatile chiral building block for peptide synthesis, enabling the construction of complex amino acid scaffolds with high stereochemical fidelity. The Fmoc group ensures efficient protection and orthogonal deprotection, while the diphenyl(p-tolyl)methyl (Dmp) amine moiety provides robust stability and facilitates selective cleavage under mild acidic conditions. This compound exhibits excellent bench stability, compatibility with standard coupling protocols, and ease of purification, making it well-suited for both academic and industrial-scale peptide assembly 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: