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Structure of 1217706-09-6
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-(thiophen-3-yl)acetic acid features a chiral α-amino acid backbone with a fluorenylmethoxycarbonyl (Fmoc) protecting group, enabling direct incorporation into peptide synthesis. The thiophen-3-yl side chain imparts enhanced solubility and electronic modulation, supporting efficient coupling under standard conditions. This bench-stable derivative facilitates the construction of complex bioactive peptides with high fidelity.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-(thiophen-3-yl)acetic acid serves as a robust chiral building block for peptide synthesis, combining the orthogonal protection of the Fmoc group with a sterically defined β-branched side chain. The thiophen-3-yl moiety imparts enhanced metabolic stability and π-stacking potential, while the bench-stable, crystalline nature facilitates straightforward purification and handling in multi-step syntheses.
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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: