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Structure of 135944-05-7
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This chiral building block features a fluorenylmethoxycarbonyl-protected amino acid scaffold with a sterically hindered α-methyl group and a phenyl-substituted β-carbon. The (S)-configuration enables stereoselective peptide synthesis, while the fluoren-9-ylmethoxycarbonyl moiety provides orthogonal protection and enhanced solubility under standard coupling conditions.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methyl-3-phenylpropanoic acid serves as a robust chiral building block for peptide synthesis, enabling efficient incorporation of sterically hindered β-branched amino acid residues. Its Fmoc group ensures excellent stability and orthogonal deprotection under mild basic conditions, while the phenyl and methyl substituents provide defined stereochemical control and enhanced structural rigidity. The compound facilitates high-yielding coupling reactions and simplifies purification through crystallization or standard chromatography.
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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: