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Structure of 252206-28-3
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This fluorenylmethoxycarbonyl-protected imidazole carboxylic acid integrates a sterically hindered, bench-stable imidazole moiety with a cleavable Fmoc group, enabling efficient incorporation into peptide chains under standard coupling conditions.
4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-1-methyl-1H-imidazole-2-carboxylic acid serves as a robust, bench-stable amino acid building block for peptide synthesis, enabling efficient N-terminal protection and orthogonal deprotection under mild conditions. The Fmoc group facilitates selective coupling in solid-phase workflows, while the imidazole-2-carboxylic acid moiety provides a versatile handle for conjugation and scaffold elaboration in medicinal chemistry applications.
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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-H320-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: