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Structure of 1018899-99-4
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This fluoren-9-ylmethoxycarbonyl (Fmoc)-protected amino acid derivative features a chiral (R)-configuration at the α-carbon, enabling stereoselective peptide synthesis. The bulky fluoren-9-ylmethyl group enhances solubility and stability during solid-phase assembly, while the pendant methyl-substituted aliphatic chain provides steric differentiation. This combination supports efficient coupling and minimizes racemization under standard conditions.
(R)-2-(((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)methyl)-4-methylpentanoic acid serves as a robust chiral building block for peptide synthesis, offering high stereoselectivity and bench stability. The Fmoc group enables efficient N-terminal protection with orthogonal deprotection under mild basic conditions, while the aliphatic side chain supports diverse functionalization. Its compatibility with standard coupling protocols and ease of purification make it ideal for solid-phase and solution-phase peptide assembly.
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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: