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Structure of 284492-07-5
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This fluorenylmethoxy carbamate-protected amino acid derivative features a sterically hindered, electron-deficient aryl moiety that enhances stability and facilitates efficient coupling in peptide synthesis. The 3-fluorophenyl group imparts favorable solubility and reduces aggregation during chain elongation.
3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-fluorophenyl)propanoic acid serves as a robust amino acid derivative for peptide synthesis, offering enhanced solubility and stability during coupling steps. The fluorenylmethoxycarbonyl (Fmoc) group enables efficient deprotection under mild basic conditions, while the 3-fluorophenyl moiety provides steric and electronic modulation for synthetic diversification. This compound facilitates reliable N-terminal protection in solid-phase and solution-phase workflows.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P501
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Lot numbers can be found on the outside label of a product: