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Structure of 284492-06-4
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This fluorenylmethoxycarbonyl-protected amino acid derivative features a sterically hindered, electron-rich aromatic moiety that enhances solubility and stability during peptide synthesis. The m-tolyl group provides robust steric shielding, minimizing racemization while the fluoren-9-ylmethoxy carbonyl (Fmoc) handle enables efficient orthogonal deprotection under mild basic conditions.
3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(m-tolyl)propanoic acid serves as a robust, bench-stable amino acid derivative for peptide synthesis, enabling efficient N-terminal protection with orthogonal deprotection under mild conditions. Its fluorenylmethoxycarbonyl (Fmoc) group provides excellent compatibility with standard coupling protocols, while the m-tolyl-substituted propanoic acid side chain enhances solubility and facilitates purification. Functions reliably 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-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: