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Structure of 180576-05-0
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This fluorenylmethoxycarbonyl-protected piperazinylacetic acid derivative serves as a key building block for peptide synthesis and bioconjugation. The Cbz-like fluorenylmethoxy carbonyl group enables selective protection of amine functionalities, while the piperazinyl scaffold imparts solubility and versatility in coupling reactions under standard conditions.
2-(4-(((9H-Fluoren-9-yl)methoxy)carbonyl)piperazin-1-yl)acetic acid serves as a robust, bench-stable building block for peptide and peptidomimetic synthesis. Its fluorenylmethoxycarbonyl (Fmoc)-protected piperazine moiety enables orthogonal functionalization and efficient incorporation into complex scaffolds. The acetic acid handle facilitates conjugation via amide bond formation, while the Fmoc group ensures high compatibility with standard solid-phase peptide synthesis protocols and simplifies purification through its distinctive UV absorbance.
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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: