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Structure of 352523-15-0
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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2-(trifluoromethyl)phenyl)propanoic acid is a chiral building block featuring a fluorenylmethoxycarbonyl (Fmoc) protected amino group and a sterically influenced trifluoromethyl-substituted aryl side chain. This configuration enables efficient incorporation into peptide synthesis workflows, offering enhanced solubility and stability under standard conditions.
(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2-(trifluoromethyl)phenyl)propanoic acid serves as a robust chiral building block for peptide synthesis, offering high stereoselectivity and bench stability. The Fmoc group enables orthogonal protection, while the trifluoromethylphenyl side chain provides enhanced metabolic stability and lipophilicity—valuable traits in medicinal chemistry. Its compatibility with standard coupling protocols and ease of purification make it a practical choice for synthesizing biologically active peptides and scaffold libraries.
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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: