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Structure of 221352-82-5
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This fluorenylmethoxycarbonyl-protected piperidine derivative features a C-terminal carboxylic acid for coupling reactions. The robust Fmoc group enables efficient solid-phase peptide synthesis, while the piperidine scaffold provides a versatile handle for modular peptide and peptidomimetic construction under standard conditions.
2-[4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)piperidin-1-yl]acetic acid serves as a versatile protected amino acid building block for peptide synthesis, enabling efficient incorporation of piperidine-derived side chains. The Fmoc group provides orthogonal protection with high stability under basic conditions and facilitates mild deprotection. Its acetic acid functionality supports conjugation via amide bond formation, while the piperidinyl moiety offers enhanced solubility and structural diversity in synthetic peptide libraries.
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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: