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Structure of 284492-08-6
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This fluorenylmethoxycarbonyl-protected amino acid derivative features a sterically hindered, electron-rich aromatic p-tolyl group and a bench-stable fluoren-9-ylmethoxy carbonyl (Fmoc) moiety. It integrates seamlessly into solid-phase peptide synthesis workflows, enabling efficient N-terminal protection with orthogonal deprotection compatibility.
3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(p-tolyl)propanoic acid serves as a robust, bench-stable amino acid derivative enabling efficient peptide coupling reactions. Its fluorenylmethyl carbamate (Fmoc) protecting group ensures orthogonal deprotection under mild basic conditions, while the p-tolyl-substituted aliphatic side chain provides steric and electronic stability. Functions effectively in solid-phase peptide synthesis, facilitating high-yielding couplings with excellent purity and minimal racemization.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: