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Structure of 313052-20-9
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This (S)-configured piperazine derivative features a fluoren-9-ylmethoxycarbonyl-protected amino group and a tert-butyl ester at the C-terminal carboxylic acid, enabling orthogonal handling in peptide synthesis. The sterically defined chiral center and electron-rich fluorenyl moiety support high-yield coupling reactions under standard conditions.
(S)-4-[2-Carboxy-2-(9H-fluoren-9-ylmethoxycarbonylamino)ethyl]piperazine-1-carboxylic acid tert-butyl ester serves as a key chiral building block for the synthesis of peptidomimetic scaffolds and bioactive heterocycles. The fluorenylmethoxycarbonyl (Fmoc) group enables orthogonal protection in solid-phase peptide synthesis, while the tert-butyl ester provides stable carboxyl protection under basic conditions. Its piperazine core offers multiple points for diversification, and the molecule exhibits excellent bench stability and ease of purification, facilitating its use in iterative coupling strategies and medicinal chemistry campaigns.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: