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Structure of 2349340-78-7
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This chiral fluorenylmethoxycarbonyl-protected amino acid derivative features a sterically hindered side chain with a 2-chloro-4-methoxyphenyl moiety, enabling high-fidelity incorporation in peptide synthesis. The (S)-configuration ensures enantioselective coupling, while the Fmoc group provides orthogonal protection and enhanced solubility under standard conditions.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2-chloro-4-methoxyphenyl)propanoic acid serves as a robust chiral building block for peptide synthesis, offering high enantiomeric purity and stability under standard coupling conditions. The Fmoc group enables efficient orthogonal deprotection, while the 2-chloro-4-methoxyphenyl side chain provides a well-defined aromatic handle compatible with diverse functionalizations. This compound facilitates reliable N-terminal protection in solid-phase peptide synthesis and supports scalable, reproducible workflows.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: