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Structure of 180181-93-5
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This fluorenylmethoxycarbonyl-protected amino acid derivative features a sterically hindered, electron-rich fluoren-9-ylmethoxy carbonyl group that enables efficient coupling in peptide synthesis. The pendant phenylpropanoic acid moiety enhances solubility and stability under standard conditions, facilitating robust N-terminal protection and subsequent deprotection without racemization.
3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-phenylpropanoic acid serves as a robust amino acid derivative for peptide synthesis, offering enhanced solubility and stability during coupling steps. The Fmoc group enables efficient deprotection under mild basic conditions, while the phenyl-substituted propanoic acid backbone provides a rigid, hydrophobic side chain useful in peptidomimetic design. Its compatibility with standard solid-phase 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,GHS08,GHS09
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Signal Word : Danger
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H319-H335-H372-H410
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Precautionary Statements : P233-P260-P261-P264-P270-P271-P273-P280-P302+P352-P304+P340-P330-P340-P362-P391-P403-P405-P501
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Lot numbers can be found on the outside label of a product: