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Structure of 1146118-59-3
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This fluorenylmethoxycarbonyl-protected glutamine derivative features a bench-stable, moisture-tolerant side chain with a dimethylated amine group at the N5 position. The Fmoc moiety enables efficient incorporation into peptide chains under standard coupling conditions, while the sterically hindered N5,N5-dimethyl substitution prevents undesired side reactions during synthesis.
N₂-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N⁵,N⁵-dimethyl-L-glutamine serves as a protected glutamine derivative with enhanced stability and solubility, enabling efficient peptide synthesis. The Fmoc group facilitates mild deprotection under basic conditions, while the N⁵,N⁵-dimethyl substitution prevents unwanted side reactions at the amide nitrogen. This structure functions reliably in solid-phase and solution-phase coupling protocols, offering excellent compatibility with standard amino acid activation methods and improving purification efficiency through distinct chromatographic behavior.
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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: