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*For research and further manufacturing use only, not for direct human use.
Structure of 205526-30-3
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3,4,5-trifluorophenyl)propanoic acid features a sterically hindered chiral center and a fluorenylmethyl carbamate (Fmoc) protecting group, enabling reliable incorporation into peptide synthesis. The trifluorophenyl moiety imparts enhanced electron-withdrawing character and metabolic stability, facilitating efficient coupling under standard conditions.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3,4,5-trifluorophenyl)propanoic acid serves as a robust chiral building block for peptide synthesis, offering enhanced stability and orthogonal protection. The Fmoc group enables efficient deprotection under mild conditions, while the trifluorophenyl side chain provides strong electron-withdrawing character and improved solubility. This derivative facilitates straightforward coupling reactions and is well-suited for solid-phase and solution-phase workflows in medicinal chemistry and API development.
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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: