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Structure of 2250198-69-5
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This fluorenylmethoxycarbonyl-protected amino acid derivative features a sterically hindered side chain and a bench-stable carbamate linkage, enabling efficient incorporation into peptide synthesis workflows. The fluoren-9-ylmethoxy carbonyl group facilitates clean deprotection under mild conditions.
2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-methylpentanoic acid serves as a robust amino acid derivative for peptide synthesis, offering enhanced solubility and stability during coupling steps. The Fmoc group enables efficient, orthogonal deprotection under mild basic conditions, while the branched aliphatic side chain minimizes aggregation and supports high-yielding reactions in solid-phase workflows. Its compatibility with standard coupling reagents and ease of purification make it a practical choice for complex peptide assembly.
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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: