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Structure of 882847-19-0
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This fluorenylmethoxycarbonyl-protected amino acid derivative features a cyclohexyl-substituted acetic acid side chain, enabling incorporation into peptide sequences with enhanced stability. The bulky fluoren-9-ylmethoxycarbonyl group provides efficient protection and facile removal under mild conditions, ideal for solid-phase peptide synthesis workflows.
2-{1-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]cyclohexyl}acetic acid serves as a versatile building block for peptide and peptidomimetic synthesis, enabling efficient incorporation of functionalized cyclohexyl motifs. The fluorenylmethoxycarbonyl (Fmoc) group provides excellent orthogonal protection for primary amines, while the pendant carboxylic acid facilitates coupling reactions under standard conditions. Its bench-stable nature and compatibility with diverse reaction environments make it ideal for solid-phase and solution-phase workflows in medicinal chemistry and API development.
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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: