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Structure of 212688-54-5
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(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-methylhexanoic acid is a chiral amino acid derivative featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group. This configuration ensures high enantioselectivity in peptide synthesis, enabling efficient incorporation into oligopeptides under standard coupling conditions. The molecule combines excellent solubility with bench-stable handling characteristics, streamlining purification and automation workflows in solid-phase peptide synthesis.
(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-methylhexanoic acid serves as a robust chiral building block for peptide synthesis, enabling efficient N-terminal protection with orthogonal deprotection under mild conditions. The Fmoc group ensures high stability during storage and handling, while the branched aliphatic side chain provides steric differentiation useful in conformationally constrained peptide design. Facilitates straightforward purification and compatibility with standard solid-phase protocols.
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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: