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Structure of 1172127-44-4
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2-fluorophenyl)-2-methylpropanoic acid is a chiral building block featuring a fluorenylmethyl carbamate (Fmoc) protecting group and a sterically hindered β-branched side chain. This configuration enables efficient incorporation into peptide synthesis workflows, where the Fmoc moiety facilitates orthogonal deprotection under mild basic conditions. The para-fluorophenyl substituent imparts enhanced solubility and stability during coupling steps.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2-fluorophenyl)-2-methylpropanoic acid serves as a robust chiral building block for peptide synthesis, enabling efficient incorporation of sterically hindered, fluorinated amino acid motifs. The Fmoc group ensures orthogonal protection and facile deprotection under mild basic conditions, while the (S)-configuration provides stereochemical control in macrocyclic and peptidomimetic scaffolds. Bench-stable and amenable to standard coupling protocols, it facilitates reliable synthesis of complex bioactive peptides and pharmaceutical 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: