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Structure of 284492-03-1
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This fluorenylmethoxycarbonyl-protected amino acid derivative features a sterically hindered, electron-rich aromatic core and a pendant o-tolyl group that enhances solubility and stability. It integrates seamlessly into peptide synthesis workflows, offering robust protection for amine functionalities under standard conditions.
3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(o-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 o-tolyl-substituted proline analog facilitates structural diversity in peptidomimetic synthesis. The molecule exhibits excellent solubility and purification compatibility, making it well-suited for solid-phase peptide synthesis and medicinal chemistry applications requiring precise side-chain functionalization.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: