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Structure of 2416720-26-6
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N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-7-methoxy-L-tryptophan is a protected amino acid derivative featuring a fluorenylmethoxycarbonyl group at the α-amino terminus and a methoxy substituent at the indole C7 position. This configuration enhances solubility in organic solvents and provides stability during peptide synthesis, enabling efficient incorporation into sequence-defined polypeptides under standard coupling conditions.
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-7-methoxy-L-tryptophan serves as a protected amino acid building block for the synthesis of peptide conjugates and biologically active heterocycles. The Fmoc group enables orthogonal protection compatible with standard solid-phase peptide synthesis, while the 7-methoxy substitution on the indole ring enhances metabolic stability and modulates electronic properties. This derivative exhibits excellent bench stability, facilitates efficient purification, and participates reliably in coupling reactions under mild conditions, making it a practical choice for complex molecule 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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: