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Structure of 507472-24-4
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This fluoren-9-ylmethoxycarbonyl-protected amino acid derivative features a chiral (S)-configuration and incorporates a para-cyanophenyl group, enhancing its utility in peptide synthesis. The Cbz moiety provides robust protection for amine functionalities, enabling selective deprotection under standard hydrogenolysis conditions. This structure facilitates efficient incorporation into peptidomimetics and bioactive oligomers.
(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-cyanophenyl)propanoic acid serves as a robust chiral building block for peptide synthesis, enabling efficient N-terminal protection with orthogonal deprotection under mild conditions. The Fmoc group ensures high stability and ease of purification, while the pendant nitrile facilitates downstream functionalization. This compound exhibits excellent solubility and compatibility in standard coupling protocols, making it well-suited for solid-phase and solution-phase peptide 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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: