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*For research and further manufacturing use only, not for direct human use.
Structure of 1210830-60-6
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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)butanoic acid features a chiral, bench-stable amino acid scaffold with orthogonal protection. The fluorenylmethyl carbamate (Fmoc) group enables efficient solid-phase peptide synthesis, while the methylated amine prevents racemization. This derivative integrates cleanly into complex peptide sequences under standard coupling conditions.
(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)butanoic acid serves as a robust chiral building block for peptide synthesis, enabling efficient Nα-acylation with high stereochemical fidelity. The Fmoc-methylamino moiety provides excellent stability under basic conditions and facilitates straightforward deprotection. Its pendant butanoic acid side chain supports diverse functionalization, making it well-suited for the construction of complex peptide scaffolds and medicinal chemistry intermediates.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: